Lifelong left ventricular remodeling of hypertrophic cardiomyopathy caused by a founder frameshift deletion mutation in the cardiac Myosin-binding protein C gene among Japanese
about
A human MYBPC3 mutation appearing about 10 centuries ago results in a hypertrophic cardiomyopathy with delayed onset, moderate evolution but with a risk of sudden deathPacing for drug-refractory or drug-intolerant hypertrophic cardiomyopathyPacing for drug-refractory or drug-intolerant hypertrophic cardiomyopathyA common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South AsiaA founder MYBPC3 mutation results in HCM with a high risk of sudden death after the fourth decade of lifeFounder mutations in hypertrophic cardiomyopathy patients in the NetherlandsCardiac myosin binding protein C and MAP-kinase activating death domain-containing gene polymorphisms and diastolic heart failure.Adverse events in families with hypertrophic or dilated cardiomyopathy and mutations in the MYBPC3 geneSignaling and myosin-binding protein C.Identifying sarcomere gene mutations in hypertrophic cardiomyopathy: a personal historyHypertrophic cardiomyopathy: a reviewFamilial screening and genetic counselling in hypertrophic cardiomyopathy: the Rotterdam experienceTNNT2 Gene Polymorphisms are Associated with Susceptibility to Idiopathic Dilated Cardiomyopathy in Kazak and Han ChineseGenetic determinants of cardiac hypertrophy.Molecular basis of hereditary cardiomyopathy: abnormalities in calcium sensitivity, stretch response, stress response and beyond.Limited distribution of a cardiomyopathy-associated variant in IndiaLong-Term Survival Following Cardiac Arrest Without Implantable Defibrillator Protection in a Hypertrophic Cardiomyopathy Patient.Two founder mutations in the alpha-tropomyosin and the cardiac myosin-binding protein C genes are common causes of hypertrophic cardiomyopathy in the Finnish population.Compound heterozygosity deteriorates phenotypes of hypertrophic cardiomyopathy with founder MYBPC3 mutation: evidence from patients and zebrafish models.Clinical features of the dilated phase of hypertrophic cardiomyopathy in comparison with those of dilated cardiomyopathy.Relationship of basal-septal fibrosis with LV outflow tract obstruction in hypertrophic cardiomyopathy: insights from cardiac magnetic resonance analysis.Heterozygous junctophilin-2 (JPH2) p.(Thr161Lys) is a monogenic cause for HCM with heart failure
P2860
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P2860
Lifelong left ventricular remodeling of hypertrophic cardiomyopathy caused by a founder frameshift deletion mutation in the cardiac Myosin-binding protein C gene among Japanese
description
2005 nî lūn-bûn
@nan
2005 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Lifelong left ventricular remo ...... protein C gene among Japanese
@ast
Lifelong left ventricular remo ...... protein C gene among Japanese
@en
Lifelong left ventricular remo ...... protein C gene among Japanese
@nl
type
label
Lifelong left ventricular remo ...... protein C gene among Japanese
@ast
Lifelong left ventricular remo ...... protein C gene among Japanese
@en
Lifelong left ventricular remo ...... protein C gene among Japanese
@nl
prefLabel
Lifelong left ventricular remo ...... protein C gene among Japanese
@ast
Lifelong left ventricular remo ...... protein C gene among Japanese
@en
Lifelong left ventricular remo ...... protein C gene among Japanese
@nl
P2093
P1476
Lifelong left ventricular remo ...... protein C gene among Japanese
@en
P2093
Akinori Kimura
Hiroaki Kitaoka
Jun Takata
Makoto Okawa
Masanori Nishinaga
Naohito Yamasaki
Nobuhiko Hitomi
Takashi Furuno
Yoshihisa Matsumura
P304
P356
10.1016/J.JACC.2005.05.087
P407
P577
2005-11-01T00:00:00Z