(Q47877602)

6 February 2018

title

Yield of genetic testing in hypertrophic cardiomyopathy (English)

1 reference

6 February 2018

4

Bernard J Gersh

1 reference

6 February 2018

Michael J Ackerman

5

object named as

Michael J Ackerman

1 reference

6 February 2018

author name string

Sara L Van Driest

1

1 reference

6 February 2018

Steve R Ommen

2

1 reference

6 February 2018

A Jamil Tajik

3

1 reference

6 February 2018

language of work or name

English

0 references

publication date

1 June 2005

1 reference

6 February 2018

published in

Mayo Clin Proc

1 reference

6 February 2018

volume

80

1 reference

6 February 2018

issue

6

1 reference

6 February 2018

page(s)

739-744

1 reference

6 February 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0025-6196%2811%2961527-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0025-6196%2811%2961527-9

7 January 2021

Identification of the genotypes causing hypertrophic cardiomyopathy in northern Sweden

1 reference

https://api.crossref.org/works/10.1016%2FS0025-6196%2811%2961527-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0025-6196%2811%2961527-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0025-6196%2811%2961527-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0025-6196%2811%2961527-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0025-6196%2811%2961527-9

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

https://api.crossref.org/works/10.1016%2FS0025-6196%2811%2961527-9

7 January 2021

Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0025-6196%2811%2961527-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0025-6196%2811%2961527-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0025-6196%2811%2961527-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0025-6196%2811%2961527-9

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

1 reference

https://api.crossref.org/works/10.1016%2FS0025-6196%2811%2961527-9

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

1 reference

https://api.crossref.org/works/10.1016%2FS0025-6196%2811%2961527-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0025-6196%2811%2961527-9

7 January 2021

Natural history of hypertrophic cardiomyopathy in the elderly

1 reference

https://api.crossref.org/works/10.1016%2FS0025-6196%2811%2961527-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0025-6196%2811%2961527-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0025-6196%2811%2961527-9

7 January 2021

Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderly

1 reference

https://api.crossref.org/works/10.1016%2FS0025-6196%2811%2961527-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0025-6196%2811%2961527-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0025-6196%2811%2961527-9

7 January 2021

Denaturing high-performance liquid chromatography: A review

1 reference

https://api.crossref.org/works/10.1016%2FS0025-6196%2811%2961527-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0025-6196%2811%2961527-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0025-6196%2811%2961527-9

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

1 reference

https://api.crossref.org/works/10.1016%2FS0025-6196%2811%2961527-9

7 January 2021

10.1016/S0025-6196(11)61527-9

Identifiers

DOI

0 references

1 reference

6 February 2018