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Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy
UploadDefects of Vps15 in skeletal muscles lead to autophagic vacuolar myopathy and lysosomal disease
Download from doi.orgVMA21 deficiency prevents vacuolar ATPase assembly and causes autophagic vacuolar myopathy
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