Protein and genetic diagnosis of limb girdle muscular dystrophy type 2A: The yield and the pitfalls
Author:
Affiliation:
1. Department of Neurosciences; Biomedical Campus “Pietro d'Abano,” via Giuseppe Orus 2B; 35129 Padova Italy
2. Fondazione Ospedale San Camillo IRCCS; Venice Italy
Publisher
Wiley
Subject
Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/mus.24682/fullpdf
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3. CAPN3 mutations in patients with idiopathic eosinophilic myositis;Krahn;Ann Neurol,2006
4. Eosinophilic infiltration related to CAPN3 mutations: a pathophysiological component of primary calpainopathy?;Krahn;Clin Genet,2011
5. Calpainopathy and eosinophilic myositis;Brown;Ann Neurol,2006
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