Modulation of Myotilin and Fylamin C in Various Muscle Diseases: A Microarray Analysis
Schematic representation of Filamin C shown as a dimer with missense... | Download Scientific Diagram
Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy | Nature Communications
Force-Dependent Structural Changes of Filamin C Rod Domains Regulated by Filamin C Dimer | Journal of the American Chemical Society
Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies | Journal of the American College of Cardiology
Missense Mutations in the FLNC Gene Causing Familial Restrictive Cardiomyopathy | Circulation: Genomic and Precision Medicine
Filamin C Cardiomyopathy Variants Cause Protein and Lysosome Accumulation | Circulation Research
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
FLNC (gene) - Wikipedia
A mutation update for the FLNC gene in myopathies and cardiomyopathies - Verdonschot - 2020 - Human Mutation - Wiley Online Library
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 - Verdonschot - 2020 - Human Mutation - Wiley Online Library
Myocardial Disease : mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy
A map of how disease-related FLNC mutations are distributed on FLNC... | Download Scientific Diagram
FLNC and MYLK2 gene mutations in a Chinese family with different phenotypes of cardiomyopathy | medRxiv
Filamin C regulates skeletal muscle atrophy by stabilizing dishevelled-2 to inhibit autophagy and mitophagy: Molecular Therapy - Nucleic Acids
Activation of PDGFRA signaling contributes to filamin C–related arrhythmogenic cardiomyopathy | Science Advances
FLNC Gene - GeneCards | FLNC Protein | FLNC Antibody
IJMS | Free Full-Text | Structure and Function of Filamin C in the Muscle Z-Disc
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 - 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
FLNC Gene Splice Mutations Cause Dilated Cardiomyopathy – topic of research paper in Biological sciences. Download scholarly article PDF and read for free on CyberLeninka open science hub.
JCM | Free Full-Text | Cardiac Filaminopathies: Illuminating the Divergent Role of Filamin C Mutations in Human Cardiomyopathy
Screening of the Filamin C Gene in a Large Cohort of Hypertrophic Cardiomyopathy Patients | Circulation: Cardiovascular Genetics
