Article
The phenotype of calpainopathy: diagnosis based on a multidisciplinary approach.
Neuromuscular disorders : NMD - 1 Apr 2001
Pollitt C, Anderson L V, Pogue R, Davison K, Pyle A, Bushby K M
Abstract excerpt
Calpainopathy (LGMD2A) is the most common type of autosomal recessive limb-girdle muscular dystrophy. We performed a systematic clinical evaluation in 13 calpainopathy patients from 11 families, with particular attention to the pattern of muscle involvement. Eleven patients had a muscle biopsy wi...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.