MtDNA mutations are a common cause of severe disease phenotypes in children with Leigh syndrome
Keywords: زنجیر تنفسی; LS; Leigh syndrome; MAPR; Mitochondrial ATP production rate; SURF1; surfeit locus protein 1; POLGA; the catalytic subunit of mitochondrial DNA polymerase; RC; respiratory chain; Leigh syndrome; Encephalopathy; Mitochondrial disorder; Neurologic disease/di