Limb-girdle muscular dystrophy type 2A in Brazilian children

ABSTRACT Calpainopathy is an autosomal recessive limb girdle muscular dystrophy (LGMD2A) caused by mutations in CAPN3 gene. Objective To present clinical and histological findings in six children with a molecular diagnosis of LGMD2A and additionally the MRI findings in two of them. Method We ret...

Full description

Saved in:
Bibliographic Details
Main Authors: Albuquerque,Marco Antônio Veloso de, Abath Neto,Osório, Silva,Francisco Marcos Alencar da, Zanoteli,Edmar, Reed,Umbertina Conti
Format: Digital revista
Published: Academia Brasileira de Neurologia - ABNEURO 2015
Online Access:
Tags: Add Tag
No Tags, Be the first to tag this record!