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.