Identificación de mutaciones y diagnóstico molecular de portadoras en familias mexicanas con distrofia muscular Duchenne/Becker

Identificación de mutaciones y diagnóstico molecular de portadoras en familias mexicanas con distrofia muscular Duchenne/Becker

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Introducción: La Distrofia muscular de Duchenne/Becker (DMD/BMD) es la miopatía hereditaria más frecuente en las poblaciones humanas. Se caracteriza por una debilidad muscular progresiva que ocasiona, para el tipo Duchenne, la muerte por falla cardiaca y/o respiratoria durante la segunda década de l...

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Bibliographic Details
Main Authors:	S. Canizales, F. Salamanca, N. García, D. Arenas
Format:	Article
Language:	English
Published:	Universidad De La Salle Bajío 2014-11-01
Series:	Nova Scientia
Subjects:	DMD/BMD Diagnóstico Molecular PCR RT-PCR Enfermedad hereditaria humana
Online Access:	http://novascientia.delasalle.edu.mx/ojs/index.php/Nova/article/view/247

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