Novel mutations in beta-myosin heavy chain, actin and troponin-I genes associated with dilated cardiomyopathy in Indian population (original) (raw)
Coexistence of Digenic Mutations in Both Thin (TPM1) and Thick (MYH7) Filaments of Sarcomeric Genes Leads to Severe Hypertrophic Cardiomyopathy in a South Indian FHCM
Jhansi Rani
DNA and cell biology, 2015
View PDFchevron_right
Genotype phenotype correlations of cardiac beta-myosin heavy chain mutations in Indian patients with hypertrophic and dilated cardiomyopathy
Taranjit Singh Rai
Molecular and cellular …, 2009
View PDFchevron_right
Genetic and clinical profile of Indian patients of idiopathic restrictive cardiomyopathy with and without hypertrophy
Taranjit Singh Rai
Molecular and cellular …, 2009
View PDFchevron_right
Genotype-phenotype analysis in four families with mutations in β-myosin heavy chain gene responsible for familial hypertrophic cardiomyopathy
Philippe Charron
Human Mutation, 1998
View PDFchevron_right
Clinical and genetic characteristics of cardiac actin gene mutations in hypertrophic cardiomyopathy
Ib Christian Klausen
Journal of Medical Genetics, 2004
View PDFchevron_right
Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience
Ronald Deprez
European Journal of Heart Failure, 2013
View PDFchevron_right
A p.R870H mutation in the beta-cardiac myosin heavy chain 7 gene causes familial hypertrophic cardiomyopathy in several members of an Indian family
Murali Bashyam
Canadian Journal of Cardiology, 2007
View PDFchevron_right
Clinical and mutational spectrum in a cohort of 105 unrelated patients with Dilated Cardiomyopathy
Gilles Millat
European Journal of …, 2011
View PDFchevron_right
Sarcomeric Protein Mutations in Dilated Cardiomyopathy
James d. Potter
Heart Failure Reviews, 2005
View PDFchevron_right
A common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South Asia
Taranjit Singh Rai
Nature genetics, 2009
View PDFchevron_right
Genetic Basis of Dilated Cardiomyopathy
Oscar Campuzano
Advances in Cardiomyopathies, 1998
View PDFchevron_right
A novel alpha-tropomyosin mutation associates with dilated and non-compaction cardiomyopathy and diminishes actin binding
Ronald Deprez
Biochimica et biophysica acta. Molecular cell research, 2013
View PDFchevron_right
Poor Prognosis of Rare Sarcomeric Gene Variants in Patients with Dilated Cardiomyopathy
Ernesto Salcedo
Clinical and Translational Science, 2013
View PDFchevron_right
Expanded Spectrum of Gene Causing Both Hypertrophic Cardiomyopathy and Dilated Cardiomyopathy
Sachio Morimoto
Circulation Research, 2009
View PDFchevron_right
Genomic findings of hypertrophic and dilated cardiomyopathy characterized in a Thai clinical genetics service
takol chareonsirisuthigul
PLOS ONE, 2022
View PDFchevron_right
MYH7 Gene Mutations in Dilated Cardiomyopathy Patients: About 190 Cases at the Institute of Cardiology, Abidjan
Bénédicte Koné
2019
View PDFchevron_right
Worse Prognosis with Gene Mutations of Beta-myosin Heavy Chain than Myosin-Binding Protein C in Chinese Patients with Hypertrophic Cardiomyopathy
Jianwei Wang
Clinical Cardiology, 2008
View PDFchevron_right
A Family with Myh7 Mutation and Different Forms of Cardiomyopathies
Minodora Teodoru
Biomedicines
View PDFchevron_right
Mutational Analysis of MYBPC3 Gene in Dilated Cardiomyopathy Patients in North Indian Population
Om Shankar
Journal of Anatomical Sciences
View PDFchevron_right
Hypertrophyc Cardiomyopathy: Infrequent Mutation of the Cardiac Beta-Myosin Heavy-Chain Gene
Roberto Mora
Revista Española de Cardiología (English Edition), 2006
View PDFchevron_right
Genetic variations of α-cardiac actin and cardiac muscle LIM protein in hypertrophic cardiomyopathy in South India
Pratibha Nallari
Experimental and clinical cardiology, 2012
View PDFchevron_right
Mutations in hotspot region of MYH7 gene exon 23 associated with restrictive cardiomyopathy
Mitali Kapoor
View PDFchevron_right
Mutation of Arg723Gly in β-myosin heavy chain gene in five Chinese families with hypertrophic cardiomyopathy
Ningzheng Dong
Chinese Medical Journal, 2006
View PDFchevron_right
Missense mutations in the beta-myosin heavy-chain gene cause central core disease in hypertrophic cardiomyopathy
F. Cyran, Neal Epstein
Proceedings of the National Academy of Sciences, 1993
View PDFchevron_right
Genetic and phenotypic characterization of mutations in myosin-binding protein C (MYBPC3) in 81 families with familial hypertrophic cardiomyopathy: total or partial haploinsufficiency
Henning Bundgaard
European Journal of Human Genetics, 2004
View PDFchevron_right
Epidemiology of cardiomyopathy - A clinical and genetic study of dilated cardiomyopathy: The EPOCH-D study
Mitali Kapoor
Journal of the Practice of Cardiovascular Sciences, 2015
View PDFchevron_right