Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies - ScienceDirect
FLNC and MYLK2 gene mutations in a Chinese family with different phenotypes of cardiomyopathy | medRxiv
Modulation of Myotilin and Fylamin C in Various Muscle Diseases: A Microarray Analysis
FLNC (gene) - Wikipedia
FLNC Gene - GeneCards | FLNC Protein | FLNC Antibody
American Journal of Case Reports | Cardiomyopathy, Proximal Myopathy, Camptocormia, and Novel Filamin C (FLNC) Variant: A Case Report - Article abstract #932648
Activation of PDGFRA signaling contributes to filamin C–related arrhythmogenic cardiomyopathy | Science Advances
FLNC Gene - GeneCards | FLNC Protein | FLNC Antibody
FLNC Gene - GeneCards | FLNC Protein | FLNC Antibody
A map of how disease-related FLNC mutations are distributed on FLNC... | Download Scientific Diagram
A mutation update for the FLNC gene in myopathies and cardiomyopathies - Verdonschot - 2020 - Human Mutation - Wiley Online Library
FLNC variants identified in patients of the Belgian FTD cohort. a... | Download Scientific Diagram
Cells | Free Full-Text | Novel Filamin C Myofibrillar Myopathy Variants Cause Different Pathomechanisms and Alterations in Protein Quality Systems
Structure of the FLNC gene and filamin C protein. (a) Within the human... | Download Scientific Diagram
The ceRNA network of FLNC gene. (A) Yellow ellipse represents FLNC,... | Download Scientific Diagram
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
Force-Dependent Structural Changes of Filamin C Rod Domains Regulated by Filamin C Dimer | Journal of the American Chemical Society
Schematic representation of Filamin C shown as a dimer with missense... | Download Scientific Diagram
A mutation update for the FLNC gene in myopathies and cardiomyopathies - Verdonschot - 2020 - Human Mutation - Wiley Online Library
In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathy | European Journal of Human Genetics
FLNC and MYLK2 gene mutations in a Chinese family with different phenotypes of cardiomyopathy | medRxiv
A mutation update for the FLNC gene in myopathies and cardiomyopathies | Scholarly Publications
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
JCM | Free Full-Text | Cardiac Filaminopathies: Illuminating the Divergent Role of Filamin C Mutations in Human Cardiomyopathy
