Filamin-C variant-associated cardiomyopathy: A pooled analysis of individual patient data to evaluate the clinical profile and risk of sudden cardiac death - Heart Rhythm
Filamin C Cardiomyopathy Variants Cause Protein and Lysosome Accumulation | Circulation Research
Novel Mutation in FLNC (Filamin C) Causes Familial Restrictive Cardiomyopathy | Semantic Scholar
Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies - ScienceDirect
A mutation update for the FLNC gene in myopathies and cardiomyopathies - Verdonschot - 2020 - Human Mutation - Wiley Online Library
FLNC Gene Splice Mutations Cause Dilated Cardiomyopathy | JACC: Basic to Translational Science
Modulation of Myotilin and Fylamin C in Various Muscle Diseases: A Microarray Analysis
Mutation profile of FLNC gene and its prognostic relevance in patients with hypertrophic cardiomyopathy - Cui - 2018 - Molecular Genetics & Genomic Medicine - Wiley Online Library
What is FLNC Gene Myopathy, distal type 4 NGS Genetic DNA Test ?
Activation of PDGFRA signaling contributes to filamin C–related arrhythmogenic cardiomyopathy | Science Advances
Screening of the Filamin C Gene in a Large Cohort of Hypertrophic Cardiomyopathy Patients | Circulation: Cardiovascular Genetics
A mutation update for the FLNC gene in myopathies and cardiomyopathies - Verdonschot - 2020 - Human Mutation - Wiley Online Library
FLNC Gene Splice Mutations Cause Dilated Cardiomyopathy - ScienceDirect
A mutation update for the FLNC gene in myopathies and cardiomyopathies - Verdonschot - 2020 - Human Mutation - Wiley Online Library
Structure of the FLNC gene and filamin C protein. (a) Within the human... | Download Scientific Diagram
A mutation update for the FLNC gene in myopathies and cardiomyopathies | Scholarly Publications
FLNC Gene - GeneCards | FLNC Protein | FLNC Antibody
Schematic representation of Filamin C shown as a dimer with missense... | Download Scientific Diagram
FLNC and MYLK2 gene mutations in a Chinese family with different phenotypes of cardiomyopathy | medRxiv
FLNC Gene - GeneCards | FLNC Protein | FLNC Antibody
In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathy | European Journal of Human Genetics
FLNC variants identified in patients of the Belgian FTD cohort. a... | Download Scientific Diagram
Activation of PDGFRA signaling contributes to filamin C–related arrhythmogenic cardiomyopathy | Science Advances
American Journal of Case Reports | Cardiomyopathy, Proximal Myopathy, Camptocormia, and Novel Filamin C (FLNC) Variant: A Case Report - Article abstract #932648
