Mitochondrial genome variation in male LHON patients with the m.11778G > A mutation

Leber hereditary optic neuropathy (LHON) is a mitochondrial disorder with symptoms limited to a single tissue, optic nerve, resulting in vision loss. In the majority of cases it is caused by one of three point mutations in mitochondrial DNA (mtDNA) but their presence is not sufficient for disease de...

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Bibliografske podrobnosti
izdano v:Metab Brain Dis
Main Authors: Piotrowska-Nowak, Agnieszka, Krawczyński, Maciej R., Kosior-Jarecka, Ewa, Ambroziak, Anna M., Korwin, Magdalena, Ołdak, Monika, Tońska, Katarzyna, Bartnik, Ewa
Format: Artigo
Jezik:Inglês
Izdano: Springer US 2020
Teme:
Original Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC7584531/
https://ncbi.nlm.nih.gov/pubmed/32740724
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11011-020-00605-3
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