Α rare case of myopathy, lactic acidosis, and severe rhabdomyolysis, due to a homozygous mutation of the ferredoxin‐2 (FDX2) gene
Article in American Journal of Medical Genetics Part A (August 2023)
The most recent citing publications are shown below. View all 2 publications that cite this research output on Dimensions.
Indentification of novel MSTO1 compound heterozygous mutations in a Chinese family with recessive cerebellar atrophy and ataxia
Article in Frontiers in Neurology (November 2022)