Mutation profile of FLNC gene and its prognostic relevance in patients with hypertrophic cardiomyopathy
Published 2018 View Full Article
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Title
Mutation profile of FLNC
gene and its prognostic relevance in patients with hypertrophic cardiomyopathy
Authors
Keywords
-
Journal
Molecular Genetics & Genomic Medicine
Volume 6, Issue 6, Pages 1104-1113
Publisher
Wiley
Online
2018-11-09
DOI
10.1002/mgg3.488
References
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Related references
Note: Only part of the references are listed.- Screening of the Filamin C Gene in a Large Cohort of Hypertrophic Cardiomyopathy PatientsCLINICAL PERSPECTIVE
- (2017) Juan Gómez et al. Circulation-Cardiovascular Genetics
- Congenital dilated cardiomyopathy caused by biallelic mutations in Filamin C
- (2016) Eyal Reinstein et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Spectrum of Mutations in Hypertrophic Cardiomyopathy Genes Among Tunisian Patients
- (2016) Nawel Jaafar et al. Genetic Testing and Molecular Biomarkers
- Mutations inFLNCare Associated with Familial Restrictive Cardiomyopathy
- (2016) Andreas Brodehl et al. HUMAN MUTATION
- Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies
- (2016) Martín F. Ortiz-Genga et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Hypertrophic remodelling in cardiac regulatory myosin light chain (MYL2) founder mutation carriers
- (2015) Godelieve R.F. Claes et al. EUROPEAN HEART JOURNAL
- Targeted Analysis of Whole Genome Sequence Data to Diagnose Genetic Cardiomyopathy
- (2014) J. R. Golbus et al. Circulation-Cardiovascular Genetics
- 2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy
- (2014) EUROPEAN HEART JOURNAL
- Malignant effects of multiple rare variants in sarcomere genes on the prognosis of patients with hypertrophic cardiomyopathy
- (2014) Jizheng Wang et al. EUROPEAN JOURNAL OF HEART FAILURE
- Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy
- (2014) Rafael Valdés-Mas et al. Nature Communications
- Filamin C-related myopathies: pathology and mechanisms
- (2012) Dieter O. Fürst et al. ACTA NEUROPATHOLOGICA
- Penetrance of Hypertrophic Cardiomyopathy in Children and Adolescents
- (2012) Morten K. Jensen et al. CIRCULATION
- Novel FLNC mutation in a patient with myofibrillar myopathy in combination with late-onset cerebellar ataxia
- (2012) Giorgio Tasca et al. MUSCLE & NERVE
- Mutations in the N-terminal Actin-Binding Domain of Filamin C Cause a Distal Myopathy
- (2011) Rachael M. Duff et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Identifying Sarcomere Gene Mutations in Hypertrophic Cardiomyopathy
- (2011) Christine E. Seidman et al. CIRCULATION RESEARCH
- Distal myopathy with upper limb predominance caused by filamin C haploinsufficiency
- (2011) V. Guergueltcheva et al. NEUROLOGY
- P2.18 A novel missense FLNC mutation causes arrhythmia and late onset myofibrillar myopathy with particular histopathology features
- (2010) D. Avila-Smirnow et al. NEUROMUSCULAR DISORDERS
- A novel heterozygous deletion–insertion mutation (2695–2712 del/GTTTGT ins) in exon 18 of the filamin C gene causes filaminopathy in a large Chinese family
- (2010) Xinghua Luan et al. NEUROMUSCULAR DISORDERS
- In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathy
- (2008) Alexey Shatunov et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Shared Genetic Causes of Cardiac Hypertrophy in Children and Adults
- (2008) Hiroyuki Morita et al. NEW ENGLAND JOURNAL OF MEDICINE
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