Mutations in sarcomeric genes MYH7, MYBPC3, TNNT2, TNNI3, and TPM1 in patients with hypertrophic cardiomyopathy (Q44089596)

29 November 2017

title

Mutations in sarcomeric genes MYH7, MYBPC3, TNNT2, TNNI3, and TPM1 in patients with hypertrophic cardiomyopathy (English)

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29 November 2017

9

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29 November 2017

2

Eliecer Coto

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29 November 2017

Mónica García-Castro

1

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29 November 2017

Julián R Reguero

3

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29 November 2017

José R Berrazueta

4

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29 November 2017

Victoria Alvarez

5

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29 November 2017

Belén Alonso

6

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29 November 2017

Rocío Sainz

7

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29 November 2017

María Martín

8

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29 November 2017

language of work or name

Spanish

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publication date

1 January 2009

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Revista Española de Cardiología

29 November 2017

published in

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29 November 2017

volume

62

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29 November 2017

issue

1

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29 November 2017

page(s)

48-56

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Hypertrophic cardiomyopathy: a systematic review

29 November 2017

cites work

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7 January 2021

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

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Phenotypic diversity in hypertrophic cardiomyopathy

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7 January 2021

Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1

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7 January 2021

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation

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Preclinical diagnosis of familial hypertrophic cardiomyopathy by genetic analysis of blood lymphocytes

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7 January 2021

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

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7 January 2021

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

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https://api.crossref.org/works/10.1016/S0300-8932(09)70020-X

7 January 2021

Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy

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7 January 2021

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

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7 January 2021

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere

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7 January 2021

Mutation spectrum in a large cohort of unrelated consecutive patients with hypertrophic cardiomyopathy

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7 January 2021

Prevalence and age-dependence of malignant mutations in the beta-myosin heavy chain and troponin T genes in hypertrophic cardiomyopathy: a comprehensive outpatient perspective

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7 January 2021

Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy

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7 January 2021

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

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7 January 2021

Development of left ventricular hypertrophy in adults in hypertrophic cardiomyopathy caused by cardiac myosin-binding protein C gene mutations

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7 January 2021

Sudden death due to troponin T mutations

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7 January 2021

Clinical manifestations of hypertrophic cardiomyopathy with mutations in the cardiac beta-myosin heavy chain gene or cardiac troponin T gene

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7 January 2021

Functional analyses of troponin T mutations that cause hypertrophic cardiomyopathy: insights into disease pathogenesis and troponin function

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7 January 2021

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

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7 January 2021

Clinical implications of hypertrophic cardiomyopathy associated with mutations in the alpha-tropomyosin gene

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7 January 2021

Clinical Features of Hypertrophic Cardiomyopathy Caused by Mutation of a “Hot Spot” in the Alpha-Tropomyosin Gene

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7 January 2021

Frequency and clinical expression of cardiac troponin I mutations in 748 consecutive families with hypertrophic cardiomyopathy.

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7 January 2021

Cellular and molecular aspects of familial hypertrophic cardiomyopathy caused by mutations in the cardiac troponin I gene

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7 January 2021

Variable clinical manifestation of a novel missense mutation in the alpha-tropomyosin (TPM1) gene in familial hypertrophic cardiomyopathy

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7 January 2021

American College of Cardiology/European Society of Cardiology Clinical Expert Consensus Document on Hypertrophic Cardiomyopathy. A report of the American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents and the Europ

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7 January 2021

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

1 reference

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7 January 2021

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

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7 January 2021

Prevalence and spectrum of mutations in the sarcomeric troponin T and I genes in a cohort of Spanish cardiac hypertrophy patients

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7 January 2021

[Beta-myosin heavy-chain gene mutations in patients with hypertrophic cardiomyopathy]

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7 January 2021

[High-risk hypertrophic cardiomyopathy associated with a novel mutation in cardiac Myosin-binding protein C]

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7 January 2021

[Hypertrophic cardiomyopathy: infrequent mutation of the cardiac beta-myosin heavy-chain gene].

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7 January 2021

Direct detection of malignant mutations in patients with hypertrophic cardiomyopathy

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https://api.crossref.org/works/10.1016/S0300-8932(09)70020-X

7 January 2021

10.1016/S0300-8932(09)70020-X

Identifiers

DOI

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29 November 2017

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