Branched-chain amino acid metabolism: from rare Mendelian diseases to more common disorders.

Human molecular genetics2014Burrage LC, Nagamani SC, Campeau PM, et al.

Study designReview

SubjectHuman & animal

Abstract

cc by 以外（cc by-nc / cc by-nc-nd / NONE 等）は抄録を再掲しない。DOI/PMID へのリンクのみ表示する。

MeSH

3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide)Amino Acids, Branched-ChainAnimalsDisease Models, AnimalHumansLiver TransplantationMaple Syrup Urine Disease

DOI 10.1093/hmg/ddu123

PMID 24651065

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