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 mutation update for the FLNC gene in myopathies and cardiomyopathies | Scholarly Publications
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
American Journal of Case Reports | Cardiomyopathy, Proximal Myopathy, Camptocormia, and Novel Filamin C (FLNC) Variant: A Case Report - Article abstract #932648
Screening of the Filamin C Gene in a Large Cohort of Hypertrophic Cardiomyopathy Patients | Circulation: Cardiovascular Genetics
Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies - ScienceDirect
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
Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies - ScienceDirect
Structure of the FLNC gene and filamin C protein. (a) Within the human... | Download Scientific Diagram
Filamin C Cardiomyopathy Variants Cause Protein and Lysosome Accumulation | Circulation Research
Filamin C Cardiomyopathy Variants Cause Protein and Lysosome Accumulation | Circulation Research
FLNC Gene Splice Mutations Cause Dilated Cardiomyopathy - ScienceDirect
FLNC Gene - GeneCards | FLNC Protein | FLNC Antibody
Force-Dependent Structural Changes of Filamin C Rod Domains Regulated by Filamin C Dimer | Journal of the American Chemical Society
Cells | Free Full-Text | Novel Filamin C Myofibrillar Myopathy Variants Cause Different Pathomechanisms and Alterations in Protein Quality Systems
Activation of PDGFRA signaling contributes to filamin C–related arrhythmogenic cardiomyopathy | Science Advances
Novel Mutation in FLNC (Filamin C) Causes Familial Restrictive Cardiomyopathy | Semantic Scholar
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
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) - Wikipedia
