论文信息 - 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 - 字舞流文

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

T. Taketani | Y. Hasegawa | Hironori Kobayashi | S. Yamaguchi | Kenji Yamada | R. Bo | Yuichi Mushimoto | Yoshimitsu Osawa | S. Yamaguchi