Phenotypic behavior of caveolin-3 mutations that cause autosomal dominant limb girdle muscular dystrophy (LGMD-1C). Retention of LGMD-1C caveolin-3 mutants within the golgi complex

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Details 詳細情報について

  • CRID
    1571135651712995840
  • NII Article ID
    80011300974
  • Data Source
    • CiNii Articles

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