IJMS | Free Full-Text | Structure and Function of Filamin C in the Muscle Z-Disc
FLNC Gene Splice Mutations Cause Dilated Cardiomyopathy - ScienceDirect
Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies - ScienceDirect
Filamin C Cardiomyopathy Variants Cause Protein and Lysosome Accumulation | Circulation Research
A mutation update for the FLNC gene in myopathies and cardiomyopathies | Scholarly Publications
A map of how disease-related FLNC mutations are distributed on FLNC... | Download Scientific Diagram
What is FLNC Gene Myopathy, distal type 4 NGS Genetic DNA Test ?
FLNC Gene - GeneCards | FLNC Protein | FLNC Antibody
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
Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy | Nature Communications
FLNC variants identified in patients of the Belgian FTD cohort. a... | Download Scientific Diagram
In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathy | European Journal of Human Genetics
JCM | Free Full-Text | Cardiac Filaminopathies: Illuminating the Divergent Role of Filamin C Mutations in Human Cardiomyopathy
American Journal of Case Reports | Cardiomyopathy, Proximal Myopathy, Camptocormia, and Novel Filamin C (FLNC) Variant: A Case Report - Article abstract #932648
Modulation of Myotilin and Fylamin C in Various Muscle Diseases: A Microarray Analysis
FLNC Gene - GeneCards | FLNC Protein | FLNC Antibody
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.
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
Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies | Journal of the American College of Cardiology
Mutation profile of FLNC gene and its prognostic relevance in patients with hypertrophic cardiomyopathy - Cui - 2018 - Molecular Genetics & Genomic Medicine - Wiley Online Library
FLNC and MYLK2 gene mutations in a Chinese family with different phenotypes of cardiomyopathy | medRxiv
FLNC Gene Splice Mutations Cause Dilated Cardiomyopathy | JACC: Basic to Translational Science
FLNC and MYLK2 gene mutations in a Chinese family with different phenotypes of cardiomyopathy | medRxiv
Filamin C Cardiomyopathy Variants Cause Protein and Lysosome Accumulation | Circulation Research
Activation of PDGFRA signaling contributes to filamin C–related arrhythmogenic cardiomyopathy | Science Advances
Structure of the FLNC gene and filamin C protein. (a) Within the human... | Download Scientific Diagram
Activation of PDGFRA signaling contributes to filamin C–related arrhythmogenic cardiomyopathy | Science Advances
Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy | Nature Communications
