A rare case of centronuclear myopathy with DNM2 mutation: genotype-phenotype correlation

Fuente: Redalyc

Saved in:

Bibliographic Details
Main Author:	Amir Ghorbani Aghbolaghi
Format:	Artículo científico
Language:	en
Published:	Hospital Universitário da Universidade de São Paulo 2017
Subjects:	Medicina DNM2 Myopathy Congenital Centronuclear
Online Access:	Acceder al recurso 1 Acceder al recurso 2 Acceder al recurso 3 Acceder al recurso 4 Acceder al recurso 5
Tags:	Add Tag No Tags, Be the first to tag this record!

Internet