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Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of the major disease-causing mutation in the α-subunit of the mitochondrial trifunctional protein

✍ Scribed by Lodewijk IJlst; Ronald J.A. Wanders; Sciichi Ushikubo; Takehiko Kamijo; Takashi Hashimoto

Book ID: 115741356
Publisher: Elsevier Science
Year: 1994
Tongue: English
Weight: 508 KB
Volume: 1215
Category: Article
ISSN: 0005-2760
DOI: 10.1016/0005-2760(94)90064-7

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