(Q28286640)

8

object named as

Bernard J Gersh

0 references

Michael J Ackerman

10

object named as

Michael J Ackerman

0 references

author name string

J Martijn Bos

1

0 references

Rainer N Poley

2

0 references

Melissa Ny

3

0 references

David J Tester

4

0 references

Xiaolei Xu

5

0 references

Matteo Vatta

6

0 references

Steve R Ommen

Molecular Genetics and Metabolism

9

0 references

language of work or name

English

0 references

publication date

May 2006

0 references

published in

0 references

volume

88

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page(s)

78-85

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issue

1

0 references

cites work

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1 reference

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Identification and functional analysis of a caveolin-3 mutation associated with familial hypertrophic cardiomyopathy

20 March 2017

1 reference

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Mutations in the muscle LIM protein and α-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosis

20 March 2017

1 reference

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Identification of the genotypes causing hypertrophic cardiomyopathy in northern Sweden

20 March 2017

1 reference

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

20 March 2017

1 reference

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The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy

20 March 2017

1 reference

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Titin mutations as the molecular basis for dilated cardiomyopathy

20 March 2017

1 reference

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Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy

20 March 2017

1 reference

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Telethonin, a novel sarcomeric protein of heart and skeletal muscle

20 March 2017

1 reference

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Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

20 March 2017

1 reference

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

20 March 2017

1 reference

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

20 March 2017

1 reference

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Titins: giant proteins in charge of muscle ultrastructure and elasticity

20 March 2017

1 reference

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

20 March 2017

1 reference

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

20 March 2017

1 reference

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Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathy

20 March 2017

1 reference

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Hypertrophic cardiomyopathy: a systematic review

29 September 2017

1 reference

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2756511

Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy

29 September 2017

1 reference

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MLP-deficient mice exhibit a disruption of cardiac cytoarchitectural organization, dilated cardiomyopathy, and heart failure

29 September 2017

1 reference

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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

29 September 2017

1 reference

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Mapping of a human LIM protein (CLP) to human chromosome 11p15.1 by fluorescence in situ hybridization

29 September 2017

1 reference

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Yield of genetic testing in hypertrophic cardiomyopathy.

29 September 2017

1 reference

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Molecular and functional characterization of a human frataxin mutation found in hypertrophic cardiomyopathy.

27 November 2018

1 reference

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Sarcomeric genotyping in hypertrophic cardiomyopathy.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2756511

W4R variant in CSRP3 encoding muscle LIM protein in a patient with hypertrophic cardiomyopathy

27 November 2018

1 reference

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

27 November 2018

1 reference

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

27 November 2018

1 reference

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

27 November 2018

1 reference

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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.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2756511

Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2756511

Spectrum of clinical phenotypes and gene variants in cardiac myosin-binding protein C mutation carriers with hypertrophic cardiomyopathy.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2756511

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

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2756511

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

27 November 2018

1 reference

Crossref

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.10.008

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

7 January 2021

1 reference

Crossref

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.10.008