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Korean Journal of Neuromuscular Disorders ; 14 : 42 - 44, December 2022 |
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Late-Onset Myopathic form of Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency Linked to Compound Heterozygous Variants in ACADVL |
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Wonjae Sung, Wonjae Sung, MD1, Young-Eun Kim, MD, PhD2, Seung Hyun Kim, MD, PhD1 |
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1Department of Neurology, College of Medicine, Hanyang University, Seoul, Korea 2Department of Laboratory Medicine, College of Medicine, Hanyang University, Seoul, Korea |
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KEYWORDS : VLCAD deficiency, Mitochondrial diseases |
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