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Korean Journal of Neuromuscular Disorders ; 14 : 42 - 44, December 2022
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
1Department of Neurology, College of Medicine, Hanyang University, Seoul, Korea 2Department of Laboratory Medicine, College of Medicine, Hanyang University, Seoul, Korea

KEYWORDS : VLCAD deficiency, Mitochondrial diseases

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