(Q50579042)

15 March 2018

title

One third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations [corrected] in MYH7 rod region. (English)

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15 March 2018

hypertrophic cardiomyopathy

main subject

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based on heuristic

inferred from title

corrigendum / erratum

Erratum: One-third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations in rod region

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author

Henning Bundgaard

3

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Paal S Andersen

8

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Lars A Larsen

Lars Allan Larsen

6

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Lars Køber

4

Lars Køber

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2

Ole Havndrup

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15 March 2018

Lotte Hougs

1

Lotte Hougs

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15 March 2018

Michael Christiansen

7

Michael Christiansen

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15 March 2018

Jens Vuust

5

Jens Vuust

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publication date

1 February 2005

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European Journal of Human Genetics

published in

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15 March 2018

volume

13

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issue

2

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page(s)

161-165

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201310

exact match

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cites work

Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201310

An online locus-specific mutation database for familial hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201310

Mutations of the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201310

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201310

Familial hypertrophic cardiomyopathy associated with a novel missense mutation affecting the ATP-binding region of the cardiac beta-myosin heavy chain

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201310

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.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201310

Genetic and phenotypic characterization of mutations in myosin-binding protein C (MYBPC3) in 81 families with familial hypertrophic cardiomyopathy: total or partial haploinsufficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201310

Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201310

Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac beta-myosin gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201310

Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201310

Adult-onset familial hypertrophic cardiomyopathy caused by a novel mutation, R694C, in the MYH7 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201310

A Novel Missense Mutation, Leu390Val, in the Cardiac ß-myosin Heavy Chain Associated with Pronounced Septal Hypertrophy in Two Families with Hypertrophic Cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201310

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%2FSJ.EJHG.5201310

21 January 2018

Identifiers

DOI

10.1038/SJ.EJHG.5201310

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15 March 2018

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15 March 2018