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Mitochondrial organization and structure are compromised in fibroblasts from patients with Huntington's disease.
Ultrastruct Pathol. 2022 Sep 3;46(5):462-475. doi: 10.1080/01913123.2022.2100951. Epub 2022 Aug 10.
Ultrastruct Pathol. 2022.
PMID: 35946926
Case report: A rare variant m.4135T>C in the MT-ND1 gene leads to Leber hereditary optic neuropathy and altered respiratory chain supercomplexes.
Rákosníková T, Kelifová S, Štufková H, Lokvencová K, Lišková P, Kousal B, Honzík T, Hansíková H, Martínek V, Tesařová M.
Rákosníková T, et al.
Front Genet. 2023 May 18;14:1182288. doi: 10.3389/fgene.2023.1182288. eCollection 2023.
Front Genet. 2023.
PMID: 37274791
Free PMC article.
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