. . . . . . . . . . . . "[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."@en . . . . . "2013-07-06"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2014-10-02T12:32:28+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .