Condition: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26


rs1114167361 in FLNC gene and CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26 PMID 21520333 2011 LOVD v.2.0: the next generation in gene variant databases.

PMID 26436962 2015 Use of Whole-Exome Sequencing for Diagnosis of Limb-Girdle Muscular Dystrophy: Outcomes and Lessons Learned.

PMID 27908349 2016 Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies.

PMID 25633252 2014 Prioritizing causal disease genes using unbiased genomic features.

PMID 26666891 2016 Mutations in FLNC are Associated with Familial Restrictive Cardiomyopathy.

rs879255640 in FLNC-AS1;FLNC gene and CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26 PMID 26666891 2016 Mutations in FLNC are Associated with Familial Restrictive Cardiomyopathy.

rs1554401581 in FLNC;FLNC-AS1 gene and CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26 PMID 27908349 2016 Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies.

PMID 28008423 2016 FLNC Gene Splice Mutations Cause Dilated Cardiomyopathy.