HSD17B10 replaces HADH2 as the approved designation for the gene mutated in 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference2 articles.
1. Inborn errors of isoleucine degradation: a review;Korman;Mol. Genet. Metab.,2006
2. Multiple functions of type 10 17beta-hydroxy- steroid dehydrogenase;Yang;Trends Endocrinol. Metab.,2005
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