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Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy
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Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countries
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Assessment of the 50 kDa dystrophin-associated glycoprotein in Brazilian patients with severe childhood autosomal recessive muscular dystrophy
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From dystrophinopathy to sarcoglycanopathy: Evolution of a concept of muscular dystrophy
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Human adhalin is alternatively spliced and the gene is located on chromosome 17q21
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