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has major subject area list
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Amino Acid Metabolism, Inborn Errors; Genes, X-Linked; Genetic Diseases, X-Linked; Host Cell Factor C1; Hyperhomocysteinemia; Mutation; Vitamin B 12
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information resource reference
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Yu HC, Sloan JL, Scharer G, Brebner A, Quintana AM, Achilly NP, Manoli I, Coughlin CR, Geiger EA, Schneck U, Watkins D, Suormala T, Van Hove JL, Fowler B, Baumgartner MR, Rosenblatt DS, Venditti CP, Shaikh TH. An X-linked cobalamin disorder caused by mutations in transcriptional coregulator HCFC1. Am J Hum Genet. 2013 Sep 05; 93(3):506-14.
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label
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An X-linked cobalamin disorder caused by mutations in transcriptional coregulator HCFC1.
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