(Q43620534)

English

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.

scientific article published in June 2001

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11377367%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

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 (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11377367%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

hypertrophic cardiomyopathy

1 reference

based on heuristic

inferred from title

familial hypertrophic cardiomyopathy

1 reference

based on heuristic

inferred from title

Paal S Andersen

3

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11377367%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

Henning Bundgaard

2

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7 November 2019

4

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7 November 2019

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O Havndrup

1

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7 November 2019

J Vuust

5

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7 November 2019

K Kjeldsen

6

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7 November 2019

M Christiansen

7

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7 November 2019

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publication date

1 June 2001

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Europe PubMed Central

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7 November 2019

American Journal of Cardiology

1 reference

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7 November 2019

87

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7 November 2019

11

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7 November 2019

1315-1317

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11377367%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2901532-6

7 January 2021

Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2901532-6

7 January 2021

A new mutation of the cardiac troponin T gene causing familial hypertrophic cardiomyopathy without left ventricular hypertrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2901532-6

7 January 2021

The molecular genetics of hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2901532-6

7 January 2021

Molecular genetic basis of hypertrophic cardiomyopathy: genetic markers for sudden cardiac death

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2901532-6

7 January 2021

Molecular genetic studies of familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2901532-6

7 January 2021

Genetic basis of cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2901532-6

7 January 2021

Experience from clinical genetics in hypertrophic cardiomyopathy: proposal for new diagnostic criteria in adult members of affected families

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2901532-6

7 January 2021

Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in a genotyped adult population.

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2901532-6

7 January 2021

Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies.

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2901532-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2901532-6

7 January 2021

Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2901532-6

7 January 2021

Genotype-phenotype correlations in hypertrophic cardiomyopathy. Insights provided by comparisons of kindreds with distinct and identical beta-myosin heavy chain gene mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2901532-6

7 January 2021

A novel deletion mutation in the beta-myosin heavy chain gene found in Japanese patients with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2901532-6

7 January 2021

Sudden cardiac death in hypertrophic cardiomyopathy. Variability in phenotypic expression of beta-myosin heavy chain mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2901532-6

7 January 2021

Sudden cardiac death in familial hypertrophic cardiomyopathy: are "benign" mutations really benign?

2 references

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2901532-6

7 January 2021

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2901532-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Hypertrophic cardiomyopathy: evaluation and treatment of patients at high risk for sudden death

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2901532-6

7 January 2021

Functional analysis of myosin mutations that cause familial hypertrophic cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2901532-6

7 January 2021

An online locus-specific mutation database for familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2901532-6

7 January 2021

The molecular biology and pathophysiology of hypertrophic cardiomyopathy due to mutations in the beta myosin heavy chains and the essential and regulatory light chains.

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2901532-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0002-9149(01)01532-6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11377367%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11377367%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

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