Matches in Nanopublications for { ?s ?p "[16 patients from 11 unrelated families were studied with a phenotype of infantile ascending hereditary spastic paralysis (IAHSP); Alsin mutations were found in 4 of the 10 families, whereas haplotype analysis excluded the ALS2 locus in one family ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP150864.RADZKaQKmaW8n3VN036lX_MZyiK5Sy_olqE-bp0HXb2L8130_assertion description "[16 patients from 11 unrelated families were studied with a phenotype of infantile ascending hereditary spastic paralysis (IAHSP); Alsin mutations were found in 4 of the 10 families, whereas haplotype analysis excluded the ALS2 locus in one family ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150864.RADZKaQKmaW8n3VN036lX_MZyiK5Sy_olqE-bp0HXb2L8130_provenance.
- NP153560.RAwZGthti-GK2JWTpb8G4hjiWhX4KdHzV10UV4JTou278130_assertion description "[16 patients from 11 unrelated families were studied with a phenotype of infantile ascending hereditary spastic paralysis (IAHSP); Alsin mutations were found in 4 of the 10 families, whereas haplotype analysis excluded the ALS2 locus in one family ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP153560.RAwZGthti-GK2JWTpb8G4hjiWhX4KdHzV10UV4JTou278130_provenance.
- NP213982.RAdakdTNXTPV7-J3lI4QG6THt-mciIJCCsaf3lDDk0sUc130_assertion description "[16 patients from 11 unrelated families were studied with a phenotype of infantile ascending hereditary spastic paralysis (IAHSP); Alsin mutations were found in 4 of the 10 families, whereas haplotype analysis excluded the ALS2 locus in one family ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213982.RAdakdTNXTPV7-J3lI4QG6THt-mciIJCCsaf3lDDk0sUc130_provenance.
- NP198337.RAUsxADcbWizL9EnFd41Mc_7QLpfMcd5YzYK7-NdlSYHE130_assertion description "[16 patients from 11 unrelated families were studied with a phenotype of infantile ascending hereditary spastic paralysis (IAHSP); Alsin mutations were found in 4 of the 10 families, whereas haplotype analysis excluded the ALS2 locus in one family ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198337.RAUsxADcbWizL9EnFd41Mc_7QLpfMcd5YzYK7-NdlSYHE130_provenance.
- NP216667.RAj8koxet72E3cr-dTsSymPKnrPff8pis2u1JA7XNtEsY130_assertion description "[16 patients from 11 unrelated families were studied with a phenotype of infantile ascending hereditary spastic paralysis (IAHSP); Alsin mutations were found in 4 of the 10 families, whereas haplotype analysis excluded the ALS2 locus in one family ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216667.RAj8koxet72E3cr-dTsSymPKnrPff8pis2u1JA7XNtEsY130_provenance.
- NP198338.RAr_SjMDNrzeGlwFcRE2gCijoLypx_-CksKsS62BMg8Xg130_assertion description "[16 patients from 11 unrelated families were studied with a phenotype of infantile ascending hereditary spastic paralysis (IAHSP); Alsin mutations were found in 4 of the 10 families, whereas haplotype analysis excluded the ALS2 locus in one family ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198338.RAr_SjMDNrzeGlwFcRE2gCijoLypx_-CksKsS62BMg8Xg130_provenance.