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A novel ACAD8 mutation in asymptomatic patients with isobutyryl‐CoA dehydrogenase deficiency and a review of the ACAD8 mutation spectrum
Authors:J.W. Yun  K.I. Jo  H.I. Woo  S.‐Y. Lee  C.‐S. Ki  J.‐W. Kim  J. Song  D.H. Lee  Y.‐W. Lee  H.‐D. Park
Affiliation:1. Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea;2. Department of Laboratory Medicine, Soonchunhyang University College of Medicine, Soonchunhyang University Bucheon Hospital, Bucheon, Republic of Korea;3. Department of Laboratory Medicine, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongam, Republic of Korea;4. Department of Pediatrics, Soonchunhyang University College of Medicine, Soonchunhyang University Hospital, Seoul, Republic of Korea
Abstract:
Keywords:
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