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

Ferruccio Galbiati, Daniela Volonté, Carlo Minetti, Jeffrey B. Chu, Michael P. Lisanti

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Medicine & Life Sciences

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