Adult-onset Repeat Rhabdomyolysis with a Very Long-chain Acyl-CoA Dehydrogenase Deficiency Due to Compound Heterozygous ACADVL Mutations.
Internal medicine (Tokyo, Japan) | 2020-11-01 | PMID 32669490
Fuseya Yasuhiro, Sakurai Takeyo, Miyahara Jun-Ichi and 8 more
