The Val606Met mutation in the cardiac beta-myosin heavy chain gene in patients with familial hypertrophic cardiomyopathy is associated with a high risk of sudden death at young age.
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Founder mutations in hypertrophic cardiomyopathy patients in the NetherlandsDiagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relativesRisk stratification for sudden cardiac death in hypertrophic cardiomyopathy: systematic review of clinical risk markers.β-Myosin heavy chain variant Val606Met causes very mild hypertrophic cardiomyopathy in mice, but exacerbates HCM phenotypes in mice carrying other HCM mutationsEvolving molecular diagnostics for familial cardiomyopathies: at the heart of it allHypertrophic cardiomyopathy: how do mutations lead to disease?Genetic variations of β-MYH7 in hypertrophic cardiomyopathy and dilated cardiomyopathy.From malignant mutations to malignant domains: the continuing search for prognostic significance in the mutant genes causing hypertrophic cardiomyopathy.One third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations [corrected] in MYH7 rod region.
P2860
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P2860
The Val606Met mutation in the cardiac beta-myosin heavy chain gene in patients with familial hypertrophic cardiomyopathy is associated with a high risk of sudden death at young age.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
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2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
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2001年學術文章
@zh-hant
name
The Val606Met mutation in the ...... of sudden death at young age.
@en
The Val606Met mutation in the ...... of sudden death at young age.
@nl
type
label
The Val606Met mutation in the ...... of sudden death at young age.
@en
The Val606Met mutation in the ...... of sudden death at young age.
@nl
prefLabel
The Val606Met mutation in the ...... of sudden death at young age.
@en
The Val606Met mutation in the ...... of sudden death at young age.
@nl
P2093
P50
P1476
The Val606Met mutation in the ...... k of sudden death at young age
@en
P2093
K Kjeldsen
M Christiansen
O Havndrup
P304
P356
10.1016/S0002-9149(01)01532-6
P407
P577
2001-06-01T00:00:00Z