FLNC-Associated Myofibrillar Myopathy

A mutation in the filamin c gene causes myofibrillar myopathy with lower motor neuron syndrome: a case report, BMC Neurology

FLNc expression in different mouse muscles, and soleus muscle of

FLNC-Associated Myofibrillar Myopathy

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

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

FLNC Gene Splice Mutations Cause Dilated Cardiomyopathy

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

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

Force-Dependent Structural Changes of Filamin C Rod Domains Regulated by Filamin C Dimer

FLNC-Associated Myofibrillar Myopathy

Myofibrillar myopathies: State of the art, present and future challenges - ScienceDirect