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[By a preliminary immunoblot screening for calpain-3 protein of 548 unclassified patients with various phenotypes (LGMD, myopathy, or elevated levels of serum creatine kinase hyperCKemia), we selected 208 cases for CAPN3 gene mutation analysis: 69 had protein deficiency and 139 had normal expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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