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

収録刊行物

• J. Biol. Chem.

  J. Biol. Chem. 274 25632-25641, 1999