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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

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