HAL (France)
open access
BIN1 overexpression rescues cardiac but not skeletal muscle defects in a mouse model of caveolinopathy
Mutations in CAV3, encoding caveolin-3, cause caveolinopathies, rare genetic disorders affecting both skeletal and cardiac muscle. Caveolin-3 contributes to T-tubule formation and excitation-contraction coupling. To date, there are no therapy for caveolinopathies. BIN1 (amphiphysin 2), a membrane-sh
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