FLNC-Associated Myofibrillar Myopathy

Filamin C regulates skeletal muscle atrophy by stabilizing dishevelled-2 to inhibit autophagy and mitophagy - ScienceDirect

FLNC Gene Splice Mutations Cause Dilated Cardiomyopathy - ScienceDirect

Frontiers Case Reports: Novel Missense Variants in the Filamin C Actin Binding Domain Cause Variable Phenotypes

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

A mutation in the dimerization domain of filamin c causes a novel type of autosomal dominant myofibrillar myopathy.

Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies - ScienceDirect

New mutation of the desmin gene identified in an extended Indian pedigree presenting with distal myopathy and cardiac disease – topic of research paper in Clinical medicine. Download scholarly article PDF and

Myofibrillar Myopathy disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials

Filamin C regulates skeletal muscle atrophy by stabilizing dishevelled-2 to inhibit autophagy and mitophagy - ScienceDirect