Mitochondrial A3243G mutation causes mitochondrial encephalomyopathy in a Chinese patient: Case report

RATIONALE: Mitochondrial mutations are associated with a wide spectrum of clinical abnormalities. More than half of these mutations are distributed in the 22 mitochondrial tRNA genes, including tRNA(Leu(UUR)). In particular, the A3243G mutation in the tRNA(Leu(UUR)) gene causes mitochondrial encepha...

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Detalles Bibliográficos
Autores principales: Liu, Xiao-Qun, Shen, Shao-Qing, Yang, Guo-Can, Liu, Qi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531061/
https://www.ncbi.nlm.nih.gov/pubmed/31083203
http://dx.doi.org/10.1097/MD.0000000000015534

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531061/
https://www.ncbi.nlm.nih.gov/pubmed/31083203
http://dx.doi.org/10.1097/MD.0000000000015534

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