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- W2334765863 abstract "Centronuclear myopathy (CM) is a heterogeneous group of congenital myopathies with onset from birth to adult ages. Autosomal recessive CM is caused by RYR1 and BIN1 (Amphiphysin) gene mutations, whereas Dynamin2 (DNM2) mutations cause dominant CM." @default.
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- W2334765863 date "2013-03-26" @default.
- W2334765863 modified "2023-09-24" @default.
- W2334765863 title "Divergence in clinical presentation of Dynamin2-caused centronuclear myopathy is associated with mutations in distinct parts of the DNM2 gene" @default.
- W2334765863 doi "https://doi.org/10.1055/s-0033-1337830" @default.
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