FLNC-Associated Myofibrillar Myopathy

Myofibrillar myopathy: MedlinePlus Genetics

Mutation profile of FLNC gene and its prognostic relevance in patients with hypertrophic cardiomyopathy - Cui - 2018 - Molecular Genetics & Genomic Medicine - Wiley Online Library

Homozygous expression of the myofibrillar myopathy-associated p.W2710X filamin C variant reveals major pathomechanisms of sarcomeric lesion formation, Acta Neuropathologica Communications

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

Analysis of a putative second dimerization region in FLNc. a

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Filamin C Cardiomyopathy Variants Cause Protein and Lysosome Accumulation

Filamin C Cardiomyopathy Variants Cause Protein and Lysosome Accumulation

Novel Mutation in FLNC (Filamin C) Causes Familial Restrictive Cardiomyopathy