Mutation profile of FLNC gene and its prognostic relevance in patients with hypertrophic cardiomyopathy - Cui - 2018 - Molecular Genetics & Genomic Medicine - Wiley Online Library
IJMS | Free Full-Text | Structure and Function of Filamin C in the Muscle Z-Disc
Activation of PDGFRA signaling contributes to filamin C–related arrhythmogenic cardiomyopathy | Science Advances
A mutation update for the FLNC gene in myopathies and cardiomyopathies | Scholarly Publications
Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy | Nature Communications
Activation of PDGFRA signaling contributes to filamin C–related arrhythmogenic cardiomyopathy | Science Advances
A map of how disease-related FLNC mutations are distributed on FLNC... | Download Scientific Diagram
FLNC Gene Splice Mutations Cause Dilated Cardiomyopathy - ScienceDirect
Multiple effect mechanisms of FLNC in dilated cardiomyopathy based on genetic variants, transcriptomics, and immune in ltration
Filamin C Cardiomyopathy Variants Cause Protein and Lysosome Accumulation | Circulation Research
FLNC (gene) - Wikipedia
Screening of the Filamin C Gene in a Large Cohort of Hypertrophic Cardiomyopathy Patients | Circulation: Cardiovascular Genetics
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 regulates skeletal muscle atrophy by stabilizing dishevelled-2 to inhibit autophagy and mitophagy: Molecular Therapy - Nucleic Acids
IJMS | Free Full-Text | Structure and Function of Filamin C in the Muscle Z-Disc
FLNC Gene - GeneCards | FLNC Protein | FLNC Antibody
FLNC variants identified in patients of the Belgian FTD cohort. a... | Download Scientific Diagram
Missense Mutations in the FLNC Gene Causing Familial Restrictive Cardiomyopathy | Circulation: Genomic and Precision Medicine
Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies | Journal of the American College of Cardiology
Filamin C Cardiomyopathy Variants Cause Protein and Lysosome Accumulation | Circulation Research
Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy | Nature Communications
Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies - ScienceDirect
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
What is FLNC Gene Myopathy, distal type 4 NGS Genetic DNA Test ?
FLNC Gene - GeneCards | FLNC Protein | FLNC Antibody
