FLNC-Associated Myofibrillar Myopathy

FLNC Gene Splice Mutations Cause Dilated Cardiomyopathy

Structure of the FLNC gene and filamin C protein. (a) Within the human

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

Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy

Muscles, Free Full-Text

FLNC-Associated Myofibrillar Myopathy

Cells, Free Full-Text

Cells, Free Full-Text

PDF) A Mutation Update for the FLNC gene in Myopathies and Cardiomyopathies

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

FLNC-Associated Myofibrillar Myopathy

Filamin C-related myopathies: pathology and mechanisms

Expanding the central nervous system disease spectrum associated with FLNC mutation - Previtali - 2019 - Muscle & Nerve - Wiley Online Library