FLNC-Associated Myofibrillar Myopathy: New Clinical, Functional, and Proteomic Data.

This new MFM-filaminopathy family confirms that expression of mutant leads to an adult-onset muscle phenotype with intracellular protein accumulation. Mutant FLNc protein is biochemically compromised and leads to dysregulation of protein quality control mechanisms. Proteomic analysis of MFM protein aggregates is a potent method to identify disease-relevant proteins, differentiate MFM subtypes, evaluate the relevance of gene variants, and identify novel MFM candidate genes.