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Neurite growth could be impaired by ETFDH mutation but restored by mitochondrial cofactors
Authors:Wen‐Chen Liang MD  Yen‐Fong Lin MSc  Ting‐Yuan Liu MSc  Shin‐Cheng Chang MSc  Bai‐Hsiun Chen MD  Ichizo Nishino MD  PhD  Yuh‐Jyh Jong MD  DMSci
Affiliation:1. Department of Pediatrics, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan;2. Department of Pediatrics, School of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan;3. Graduate Institute of Clinical Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan;4. Department of Laboratory Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan;5. Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan;6. Department of Clinical Development, Translational Medical Center, National Center of Neurology and Psychiatry, Tokyo, Japan;7. Department of Biological Science and Technology, College of Biological Science and Technology, National Chiao Tung University, Hsinchu, Taiwan
Abstract:
Keywords:carnitine  coenzyme Q10  ETFDH  lipid storage myopathy  multiple acyl‐coenzyme A dehydrogenase deficiency  neurite shortening  riboflavin
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