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Case Report: m.13513 G>A Mutation in a Chinese Patient With Both Leigh Syndrome and Wolff-Parkinson-White Syndrome

A number of causative mutations in mitochondrial and nuclear DNA have been identified for Leigh syndrome, a neurodegenerative encephalopathy, including m. 8993 T>G, m.8993 T>C, and m.3243A>G mutations in the MTATP6, MTATP6, and MT-TL1 genes, respectively, which have been reported in Leigh s...

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Detalles Bibliográficos
Autores principales: Liang, Jian-Min, Xin, Cui-Juan, Wang, Guang-Liang, Wu, Xue-Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8281295/
https://www.ncbi.nlm.nih.gov/pubmed/34277526
http://dx.doi.org/10.3389/fped.2021.700898