Broadening the phenotype of m.5703G>A mutation in mitochondrial tRNA(Asn) gene from mitochondrial myopathy to myoclonic epilepsy with ragged red fibers syndrome

Detalles Bibliográficos
Autores principales: Fu, Jun, Ma, Ming-Ming, Pang, Mi, Yang, Liang, Li, Gang, Song, Jia, Zhang, Jie-Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Correspondence
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6595846/
https://www.ncbi.nlm.nih.gov/pubmed/30897601
http://dx.doi.org/10.1097/CM9.0000000000000151

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6595846/
https://www.ncbi.nlm.nih.gov/pubmed/30897601
http://dx.doi.org/10.1097/CM9.0000000000000151

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