(Q34327150)

1 August 2017

title

The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy (English)

1 reference

1 August 2017

0 references

Paula Hedley

3

0 references

Paal S Andersen

Paal Skytt Andersen

2

0 references

Henning Bundgaard

Henning Bundgaard

5

0 references

Lars Køber

8

Lars Køber

1 reference

1 August 2017

Johanna C. Moolman-Smook

6

Johanna Moolman-Smook

1 reference

1 August 2017

7

Michael Christiansen

1 reference

1 August 2017

Daniel Vega Møller

1

1 reference

1 August 2017

Mads Kristian Ersbøll

4

1 reference

1 August 2017

publication date

18 March 2009

1 reference

European Journal of Human Genetics

1 August 2017

published in

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1 August 2017

volume

17

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1 August 2017

issue

10

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1 August 2017

page(s)

1241-1249

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Mutations in sarcomere protein genes in left ventricular noncompaction

1 August 2017

cites work

1 reference

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Hypertrophic and dilated cardiomyopathy mutations differentially affect the molecular force generation of mouse alpha-cardiac myosin in the laser trap assay

6 July 2018

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Sodium channel mutations and susceptibility to heart failure and atrial fibrillation

6 July 2018

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Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy

6 July 2018

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ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating

6 July 2018

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Genetics of hypertrophic cardiomyopathy in eastern Finland: few founder mutations with benign or intermediary phenotypes

6 July 2018

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Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction

6 July 2018

1 reference

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Mutations in the muscle LIM protein and α-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosis

6 July 2018

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Identification of the genotypes causing hypertrophic cardiomyopathy in northern Sweden

6 July 2018

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Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy

6 July 2018

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Dilated cardiomyopathy and heart failure caused by a mutation in phospholamban

6 July 2018

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The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy

6 July 2018

1 reference

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mRNA surveillance: the perfect persist

6 July 2018

1 reference

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Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderly

6 July 2018

1 reference

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Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy

6 July 2018

1 reference

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6 July 2018

1 reference

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Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy

6 July 2018

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Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease

6 July 2018

1 reference

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Desmin mutation responsible for idiopathic dilated cardiomyopathy

6 July 2018

1 reference

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6 July 2018

1 reference

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Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

6 July 2018

1 reference

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6 July 2018

1 reference

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6 July 2018

1 reference

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The Frequency of Familial Dilated Cardiomyopathy in a Series of Patients with Idiopathic Dilated Cardiomyopathy

6 July 2018

1 reference

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Frequency and phenotypes of familial dilated cardiomyopathy.

6 July 2018

1 reference

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Early death from cardiomyopathy in a family with autosomal dominant striate palmoplantar keratoderma and woolly hair associated with a novel insertion mutation in desmoplakin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.34

Metavinculin mutations alter actin interaction in dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.34

Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.34

Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.34

Novel mutations in sarcomeric protein genes in dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.34

Hypertrophic cardiomyopathy linked to homozygosity for a new mutation in the myosin-binding protein C gene (A627V) suggests a dosage effect.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.34

Identification of a metavinculin missense mutation, R975W, associated with both hypertrophic and dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.34

Dilated and hypertrophic cardiomyopathy mutations in troponin and alpha-tropomyosin have opposing effects on the calcium affinity of cardiac thin filaments

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.34

Effect of enalapril on 12-year survival and life expectancy in patients with left ventricular systolic dysfunction: a follow-up study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.34

The benefits of early combination treatment of carvedilol and an ACE-inhibitor in mild heart failure and left ventricular systolic dysfunction. The carvedilol and ACE-inhibitor remodelling mild heart failure evaluation trial (CARMEN).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.34

High-throughput single strand conformation polymorphism mutation detection by automated capillary array electrophoresis: validation of the method

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.34

Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.34

Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland

21 January 2018

1 reference

12 December 2020

Hypertrophic cardiomyopathy: low frequency of mutations in the beta-myosin heavy chain (MYH7) and cardiac troponin T (TNNT2) genes among Spanish patients

1 reference

12 December 2020

Hypertrophic cardiomyopathy: two homozygous cases with "typical" hypertrophic cardiomyopathy and three new mutations in cases with progression to dilated cardiomyopathy

1 reference

12 December 2020

Epidemiology of idiopathic dilated and hypertrophic cardiomyopathy. A population-based study in Olmsted County, Minnesota, 1975-1984

1 reference

12 December 2020

Ca2+ sensitization and potentiation of the maximum level of myofibrillar ATPase activity caused by mutations of troponin T found in familial hypertrophic cardiomyopathy

1 reference

12 December 2020

Identifiers

DOI

10.1038/EJHG.2009.34

1 reference

1 August 2017

1 reference

1 August 2017

1 reference