Yield of genetic testing in hypertrophic cardiomyopathy. (Q47877602)

6 February 2018

title

Yield of genetic testing in hypertrophic cardiomyopathy. (English)

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6 February 2018

4

Bernard J Gersh

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6 February 2018

Michael J Ackerman

5

object named as

Michael J Ackerman

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6 February 2018

author name string

Sara L Van Driest

1

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6 February 2018

Steve R Ommen

2

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6 February 2018

A Jamil Tajik

3

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6 February 2018

language of work or name

English

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publication date

1 June 2005

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6 February 2018

published in

Mayo Clin Proc

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6 February 2018

volume

80

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6 February 2018

issue

6

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6 February 2018

page(s)

739-744

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6 February 2018

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

cites work

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

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7 January 2021

Identification of the genotypes causing hypertrophic cardiomyopathy in northern Sweden

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7 January 2021

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

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7 January 2021

The cardiac troponin I gene is not associated with hypertrophic cardiomyopathy in patients from eastern Finland

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7 January 2021

The cardiac beta-myosin heavy chain gene is not the predominant gene for hypertrophic cardiomyopathy in the Finnish population.

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7 January 2021

No variants in the cardiac actin gene in Finnish patients with dilated or hypertrophic cardiomyopathy

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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

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7 January 2021

Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy.

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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

Comprehensive analysis of the beta-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy.

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A novel TPM1 mutation in a family with hypertrophic cardiomyopathy and sudden cardiac death in childhood

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7 January 2021

Prevalence and severity of "benign" mutations in the beta-myosin heavy chain, cardiac troponin T, and alpha-tropomyosin genes in hypertrophic cardiomyopathy

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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

Mutations of the beta myosin heavy chain gene in hypertrophic cardiomyopathy: critical functional sites determine prognosis

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7 January 2021

Natural history of hypertrophic cardiomyopathy in the elderly

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7 January 2021

Hypertrophic cardiomyopathy in the elderly. Distinctions from the young based on cardiac shape.

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Hypertensive hypertrophic cardiomyopathy or hypertrophic cardiomyopathy with hypertension? A study of 78 patients

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7 January 2021

Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderly

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7 January 2021

Structural analysis of the titin gene in hypertrophic cardiomyopathy: identification of a novel disease gene

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7 January 2021

Prevalence of Anderson-Fabry disease in male patients with late onset hypertrophic cardiomyopathy

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7 January 2021

Denaturing high-performance liquid chromatography: A review

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7 January 2021

DHPLC analysis as a platform for molecular diagnosis of congenital disorders of glycosylation (CDG)

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7 January 2021

Comparison of fluorescent SSCP and denaturing HPLC analysis with direct sequencing for mutation screening in hypertrophic cardiomyopathy

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7 January 2021

Mutation searching in colorectal cancer studies: experience with a denaturing high-pressure liquid chromatography system for exon-by-exon scanning of tumour suppressor genes

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7 January 2021

10.1016/S0025-6196(11)61527-9

Identifiers

DOI

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PubMed ID

15945527

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6 February 2018