Filamin C-related myopathies: pathology and mechanisms

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Cell Autophagy, Mitophagy, Muscle Function +5

Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans

Stephen P. Robertson, Stephen R.F. Twigg, Andrew J. Sutherland‐Smith et al. · Nature Genetics · 2003 · 426 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +8

Mutation in <i>BAG3</i> causes severe dominant childhood muscular dystrophy

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A Mutation in the Dimerization Domain of Filamin C Causes a Novel Type of Autosomal Dominant Myofibrillar Myopathy

Matthias Vorgerd, Peter F. M. van der Ven, Vera Bruchertseifer et al. · The American Journal of Human Genetics · 2005 · 309 citations · Full text

Mendelian Disorder, Novel Type, Genetics +6

Filamin 2 (FLN2): A Muscle-specific Sarcoglycan Interacting Protein

Terri G. Thompson, Yiu-mo Chan, Andrew A. Hack et al. · The Journal of Cell Biology · 2000 · 293 citations · Full text