Matches in Nanopublications for { ?s ?p "[Heritable mutations in the ttpA gene, encoding for TTP, result in ataxia with vitamin E deficiency (AVED) syndrome, typified by low vitamin E levels and a plethora of neurological disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP741932.RAoaKYWP9qMDRzqceBmZr6q5bOYojpEglP7xp_tE2l-_Q130_assertion description "[Heritable mutations in the ttpA gene, encoding for TTP, result in ataxia with vitamin E deficiency (AVED) syndrome, typified by low vitamin E levels and a plethora of neurological disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP741932.RAoaKYWP9qMDRzqceBmZr6q5bOYojpEglP7xp_tE2l-_Q130_provenance.
- NP400654.RA1fMPlwL6FCy1nG555GTBhymmSvcFwei9lr8y0byij8A130_assertion description "[Heritable mutations in the ttpA gene, encoding for TTP, result in ataxia with vitamin E deficiency (AVED) syndrome, typified by low vitamin E levels and a plethora of neurological disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400654.RA1fMPlwL6FCy1nG555GTBhymmSvcFwei9lr8y0byij8A130_provenance.
- NP340710.RA_n5eqk8rK2YeETsidsQSGgSm9aXInk7B2ByOLpE5jSs130_assertion description "[Heritable mutations in the ttpA gene, encoding for TTP, result in ataxia with vitamin E deficiency (AVED) syndrome, typified by low vitamin E levels and a plethora of neurological disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP340710.RA_n5eqk8rK2YeETsidsQSGgSm9aXInk7B2ByOLpE5jSs130_provenance.
- NP761491.RAVSla8aOP2c7nZ9NMJdrw3nbPPOXMkCL5F1IgLiBpBOQ130_assertion description "[Heritable mutations in the ttpA gene, encoding for TTP, result in ataxia with vitamin E deficiency (AVED) syndrome, typified by low vitamin E levels and a plethora of neurological disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761491.RAVSla8aOP2c7nZ9NMJdrw3nbPPOXMkCL5F1IgLiBpBOQ130_provenance.
- assertion description "[Heritable mutations in the ttpA gene, encoding for TTP, result in ataxia with vitamin E deficiency (AVED) syndrome, typified by low vitamin E levels and a plethora of neurological disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP558068.RAnfjeuFdipN8f_oGQf9LPEBxLX9AVn-Un7MhYKc_KA8I130_assertion description "[Heritable mutations in the ttpA gene, encoding for TTP, result in ataxia with vitamin E deficiency (AVED) syndrome, typified by low vitamin E levels and a plethora of neurological disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP558068.RAnfjeuFdipN8f_oGQf9LPEBxLX9AVn-Un7MhYKc_KA8I130_provenance.
- NP761452.RA4e5zVFE-z_I0DuDPfAPtmZwn5Me2Na11JUjwWHCMvPg130_assertion description "[Heritable mutations in the ttpA gene, encoding for TTP, result in ataxia with vitamin E deficiency (AVED) syndrome, typified by low vitamin E levels and a plethora of neurological disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761452.RA4e5zVFE-z_I0DuDPfAPtmZwn5Me2Na11JUjwWHCMvPg130_provenance.
- NP558066.RA2hN2LveOt7N9miPiHlm4rCjZTpryaHym_SJaEcSUO3Y130_assertion description "[Heritable mutations in the ttpA gene, encoding for TTP, result in ataxia with vitamin E deficiency (AVED) syndrome, typified by low vitamin E levels and a plethora of neurological disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP558066.RA2hN2LveOt7N9miPiHlm4rCjZTpryaHym_SJaEcSUO3Y130_provenance.