Subject
Genetics (clinical),Genetics,Molecular Medicine
Reference5 articles.
1. Case report: Optic atrophy and nephropathy with m.13513G>A/MT-ND5 mtDNA pathogenic variant;Barone;Front. Genet.,2022
2. Cardiovascular involvement in mtDNA disease: Diagnosis, management, and therapeutic options;Lioncino;Heart Fail Clin.,2022
3. The mitochondrial 13513G > A mutation is most frequent in Leigh syndrome combined with reduced complex I activity, optic atrophy and/or Wolff-Parkinson-White;Ruiter;Eur. J. Hum. Genet.,2007
4. MELAS/LS overlap syndrome associated with mitochondrial DNA mutations: Clinical, genetic, and radiological studies;Wei;Front. Neurol.,2021
5. TALEN-mediated shift of mitochondrial DNA heteroplasmy in MELAS-iPSCs with m.13513G>A mutation;Yahata;Sci. Rep.,2017