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Molecular Genetics and Metabolism Reports 33

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Clinical and molecular investigation of 37 Japanese patients with multiple acyl-CoA dehydrogenase deficiency: p.Y507D in ETFDH, a common Japanese variant, causes a mortal phenotype
Author YAMADA, Kenji/ Osawa, Yoshimitsu/ Kobayashi, Hironori/ Bo, Ryosuke/ Mushimoto, Yuichi/ HASEGAWA, Yuki/ Yamaguchi, Seiji/ Taketani, Takeshi/
Journal Title Molecular Genetics and Metabolism Reports
Volume 33
Published Date 2022-11-14
NII Type Journal Article
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