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Brain atrophy in a patient with mitochondrial DNA G8363A mutation

Detalles Bibliográficos
Autores principales:	Xu, Hong-Liang, Lian, Ya-Jun, Chen, Xin
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer Health 2019
Materias:	Correspondence
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6793787/ https://www.ncbi.nlm.nih.gov/pubmed/31433329 http://dx.doi.org/10.1097/CM9.0000000000000395

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