Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[We report in an affected man and his mother an adult-onset form of childhood ataxia with central nervous system hypomyelination/vanishing white matter disease-like disorder with no mutations in the EIF2B genes and normal guanine nucleotide exchange factor eIF2B activity, suggesting a new dominant inheritance of this syndrome that may involve other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP567877.RAB2iKe8BzOVJ291vvRyDeYXiqVtT6xOw-9vee4F5l6m4130_assertion description "[We report in an affected man and his mother an adult-onset form of childhood ataxia with central nervous system hypomyelination/vanishing white matter disease-like disorder with no mutations in the EIF2B genes and normal guanine nucleotide exchange factor eIF2B activity, suggesting a new dominant inheritance of this syndrome that may involve other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP567877.RAB2iKe8BzOVJ291vvRyDeYXiqVtT6xOw-9vee4F5l6m4130_provenance.
• NP530302.RAQaXQEAbMCGRg2b1ID5T6WOuTy5-_F69wWM6zEYMemwQ130_assertion description "[We report in an affected man and his mother an adult-onset form of childhood ataxia with central nervous system hypomyelination/vanishing white matter disease-like disorder with no mutations in the EIF2B genes and normal guanine nucleotide exchange factor eIF2B activity, suggesting a new dominant inheritance of this syndrome that may involve other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP530302.RAQaXQEAbMCGRg2b1ID5T6WOuTy5-_F69wWM6zEYMemwQ130_provenance.
• NP222155.RAxLMMLmQftGYyIAKx4A2ht5u2QE4S0tcGGY_X-lJFOTQ130_assertion description "[We report in an affected man and his mother an adult-onset form of childhood ataxia with central nervous system hypomyelination/vanishing white matter disease-like disorder with no mutations in the EIF2B genes and normal guanine nucleotide exchange factor eIF2B activity, suggesting a new dominant inheritance of this syndrome that may involve other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222155.RAxLMMLmQftGYyIAKx4A2ht5u2QE4S0tcGGY_X-lJFOTQ130_provenance.
• NP426777.RABhCJhF4WJjnPb8jDo-IU3K4hGhvAPQAaJgclB_tR7AQ130_assertion description "[We report in an affected man and his mother an adult-onset form of childhood ataxia with central nervous system hypomyelination/vanishing white matter disease-like disorder with no mutations in the EIF2B genes and normal guanine nucleotide exchange factor eIF2B activity, suggesting a new dominant inheritance of this syndrome that may involve other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426777.RABhCJhF4WJjnPb8jDo-IU3K4hGhvAPQAaJgclB_tR7AQ130_provenance.
• NP438545.RABIDg4Mq85VkzK3XytOaSIHCb5w_0x3-Sa197m-23MXU130_assertion description "[We report in an affected man and his mother an adult-onset form of childhood ataxia with central nervous system hypomyelination/vanishing white matter disease-like disorder with no mutations in the EIF2B genes and normal guanine nucleotide exchange factor eIF2B activity, suggesting a new dominant inheritance of this syndrome that may involve other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP438545.RABIDg4Mq85VkzK3XytOaSIHCb5w_0x3-Sa197m-23MXU130_provenance.
• NP158462.RAh9_hr3DxxnBrXOcMjfcnR38clrICVgWNtDgSLuEt2F0130_assertion description "[We report in an affected man and his mother an adult-onset form of childhood ataxia with central nervous system hypomyelination/vanishing white matter disease-like disorder with no mutations in the EIF2B genes and normal guanine nucleotide exchange factor eIF2B activity, suggesting a new dominant inheritance of this syndrome that may involve other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP158462.RAh9_hr3DxxnBrXOcMjfcnR38clrICVgWNtDgSLuEt2F0130_provenance.
• NP274774.RArbo92ipYIPLksAAhVGjFbjW06V_c2gmJXNi6yXrNRR8130_assertion description "[We report in an affected man and his mother an adult-onset form of childhood ataxia with central nervous system hypomyelination/vanishing white matter disease-like disorder with no mutations in the EIF2B genes and normal guanine nucleotide exchange factor eIF2B activity, suggesting a new dominant inheritance of this syndrome that may involve other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274774.RArbo92ipYIPLksAAhVGjFbjW06V_c2gmJXNi6yXrNRR8130_provenance.
• NP601092.RA3x7nyto-ZhQbsFDDt-4jnLDv9AVOPafymka6qYLFCFU130_assertion description "[We report in an affected man and his mother an adult-onset form of childhood ataxia with central nervous system hypomyelination/vanishing white matter disease-like disorder with no mutations in the EIF2B genes and normal guanine nucleotide exchange factor eIF2B activity, suggesting a new dominant inheritance of this syndrome that may involve other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP601092.RA3x7nyto-ZhQbsFDDt-4jnLDv9AVOPafymka6qYLFCFU130_provenance.
• NP719612.RAXgw2pqrx7YbN0vwH508Oh_YVQZt6azpKovhSqXVI3ts130_assertion description "[We report in an affected man and his mother an adult-onset form of childhood ataxia with central nervous system hypomyelination/vanishing white matter disease-like disorder with no mutations in the EIF2B genes and normal guanine nucleotide exchange factor eIF2B activity, suggesting a new dominant inheritance of this syndrome that may involve other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719612.RAXgw2pqrx7YbN0vwH508Oh_YVQZt6azpKovhSqXVI3ts130_provenance.
• NP503312.RA1cKor75ZV2-si7rCizf9tvgZtp9B4_ET5oprC64Fpx0130_assertion description "[We report in an affected man and his mother an adult-onset form of childhood ataxia with central nervous system hypomyelination/vanishing white matter disease-like disorder with no mutations in the EIF2B genes and normal guanine nucleotide exchange factor eIF2B activity, suggesting a new dominant inheritance of this syndrome that may involve other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP503312.RA1cKor75ZV2-si7rCizf9tvgZtp9B4_ET5oprC64Fpx0130_provenance.
• NP610418.RA5g0R5eEhUxOa6mify-lJjIEKQpywnmGzHPvk7Ze-A78130_assertion description "[We report in an affected man and his mother an adult-onset form of childhood ataxia with central nervous system hypomyelination/vanishing white matter disease-like disorder with no mutations in the EIF2B genes and normal guanine nucleotide exchange factor eIF2B activity, suggesting a new dominant inheritance of this syndrome that may involve other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP610418.RA5g0R5eEhUxOa6mify-lJjIEKQpywnmGzHPvk7Ze-A78130_provenance.
• assertion description "[We report in an affected man and his mother an adult-onset form of childhood ataxia with central nervous system hypomyelination/vanishing white matter disease-like disorder with no mutations in the EIF2B genes and normal guanine nucleotide exchange factor eIF2B activity, suggesting a new dominant inheritance of this syndrome that may involve other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP364475.RAEzj7YylTwT5lzeYgbkYl1ITNsPPm9Ep_20JeVuqnU3Q130_assertion description "[We report in an affected man and his mother an adult-onset form of childhood ataxia with central nervous system hypomyelination/vanishing white matter disease-like disorder with no mutations in the EIF2B genes and normal guanine nucleotide exchange factor eIF2B activity, suggesting a new dominant inheritance of this syndrome that may involve other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP364475.RAEzj7YylTwT5lzeYgbkYl1ITNsPPm9Ep_20JeVuqnU3Q130_provenance.
• NP657870.RA_CnKh542PG4O7LB8RUF-aguayJNkdbwa3RaMqkoyHAs130_assertion description "[We report in an affected man and his mother an adult-onset form of childhood ataxia with central nervous system hypomyelination/vanishing white matter disease-like disorder with no mutations in the EIF2B genes and normal guanine nucleotide exchange factor eIF2B activity, suggesting a new dominant inheritance of this syndrome that may involve other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP657870.RA_CnKh542PG4O7LB8RUF-aguayJNkdbwa3RaMqkoyHAs130_provenance.
• assertion description "[We report in an affected man and his mother an adult-onset form of childhood ataxia with central nervous system hypomyelination/vanishing white matter disease-like disorder with no mutations in the EIF2B genes and normal guanine nucleotide exchange factor eIF2B activity, suggesting a new dominant inheritance of this syndrome that may involve other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[We report in an affected man and his mother an adult-onset form of childhood ataxia with central nervous system hypomyelination/vanishing white matter disease-like disorder with no mutations in the EIF2B genes and normal guanine nucleotide exchange factor eIF2B activity, suggesting a new dominant inheritance of this syndrome that may involve other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[We report in an affected man and his mother an adult-onset form of childhood ataxia with central nervous system hypomyelination/vanishing white matter disease-like disorder with no mutations in the EIF2B genes and normal guanine nucleotide exchange factor eIF2B activity, suggesting a new dominant inheritance of this syndrome that may involve other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[We report in an affected man and his mother an adult-onset form of childhood ataxia with central nervous system hypomyelination/vanishing white matter disease-like disorder with no mutations in the EIF2B genes and normal guanine nucleotide exchange factor eIF2B activity, suggesting a new dominant inheritance of this syndrome that may involve other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[We report in an affected man and his mother an adult-onset form of childhood ataxia with central nervous system hypomyelination/vanishing white matter disease-like disorder with no mutations in the EIF2B genes and normal guanine nucleotide exchange factor eIF2B activity, suggesting a new dominant inheritance of this syndrome that may involve other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[We report in an affected man and his mother an adult-onset form of childhood ataxia with central nervous system hypomyelination/vanishing white matter disease-like disorder with no mutations in the EIF2B genes and normal guanine nucleotide exchange factor eIF2B activity, suggesting a new dominant inheritance of this syndrome that may involve other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[We report in an affected man and his mother an adult-onset form of childhood ataxia with central nervous system hypomyelination/vanishing white matter disease-like disorder with no mutations in the EIF2B genes and normal guanine nucleotide exchange factor eIF2B activity, suggesting a new dominant inheritance of this syndrome that may involve other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP929090.RAO7mn_CkfbIyDyHIwmKlFjpWbkIGIcQ9AzCoJijaGEmg130_assertion description "[We report in an affected man and his mother an adult-onset form of childhood ataxia with central nervous system hypomyelination/vanishing white matter disease-like disorder with no mutations in the EIF2B genes and normal guanine nucleotide exchange factor eIF2B activity, suggesting a new dominant inheritance of this syndrome that may involve other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP929090.RAO7mn_CkfbIyDyHIwmKlFjpWbkIGIcQ9AzCoJijaGEmg130_provenance.