关键词: EFTDH gene Gene mutation Lipid storage myopathy Multiple acyl-CoA dehydrogenase deficiency Muscle weakness Riboflavin
Mesh : Acyl-CoA Dehydrogenase / genetics Child Cytoplasmic Vesicles / pathology DNA Mutational Analysis Female Humans Multiple Acyl Coenzyme A Dehydrogenase Deficiency / genetics Mutation / genetics
来 源: DOI:10.1016/j.jns.2015.04.011