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

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Dettagli Bibliografici
Autore principale:	Amir Ghorbani Aghbolaghi
Natura:	Artículo científico
Lingua:	en
Pubblicazione:	Hospital Universitário da Universidade de São Paulo 2017
Soggetti:	Medicina DNM2 Myopathy Congenital Centronuclear
Accesso online:	Acceder al recurso 1 Acceder al recurso 2 Acceder al recurso 3 Acceder al recurso 4 Acceder al recurso 5
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