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...
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| Main Authors: | , , , , |
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| Format: | Digital revista |
| Language: | English |
| Published: |
Academia Brasileira de Neurologia - ABNEURO
2015
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| Online Access: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2015001200993 |
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