The ABCʼs of limb-girdle muscular dystrophy: α-sarcoglycanopathy, Bethlem myopathy, calpainopathy and more
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Clinical Neurology,Neurology
Reference39 articles.
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2. Dystrophinopathy in isolated cases of myopathy in females
3. Genetic counseling of isolated carriers of Duchenne muscular dystrophy
4. Autosomal recessive limbgirdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ–sarcoglycan gene
5. Abnormalities in α-, β- and γ-sarcoglycan in patients with limb-girdle muscular dystrophy
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