Clinical utility gene card for: dilated cardiomyopathy (CMD). (Q41791204)

10 October 2017

Clinical utility gene card for: dilated cardiomyopathy (CMD). (English)

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10 October 2017

dilated cardiomyopathy

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Anna Posafalvi

1

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10 October 2017

Johanna C Herkert

2

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10 October 2017

Richard J Sinke

3

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10 October 2017

Maarten P van den Berg

4

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10 October 2017

Jens Mogensen

5

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10 October 2017

Jan D H Jongbloed

6

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10 October 2017

J Peter van Tintelen

7

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10 October 2017

19 December 2012

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European Journal of Human Genetics

10 October 2017

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10 October 2017

21

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10 October 2017

10

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https://scigraph.springernature.com/pub.10.1038/ejhg.2012.276

10 October 2017

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cites work

Phospholamban R14del mutation in patients diagnosed with dilated cardiomyopathy or arrhythmogenic right ventricular cardiomyopathy: evidence supporting the concept of arrhythmogenic cardiomyopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778334

PGD for inherited cardiac diseases.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778334

Truncations of titin causing dilated cardiomyopathy.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778334

Update 2011: clinical and genetic issues in familial dilated cardiomyopathy

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778334

Rare variant mutations identified in pediatric patients with dilated cardiomyopathy

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778334

Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778334

Clinical and genetic issues in dilated cardiomyopathy: a review for genetics professionals

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778334

DNA testing for hypertrophic cardiomyopathy: a cost-effectiveness model

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778334

Compound and digenic heterozygosity contributes to arrhythmogenic right ventricular cardiomyopathy

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778334

The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778334

Guidelines for the study of familial dilated cardiomyopathies. Collaborative Research Group of the European Human and Capital Mobility Project on Familial Dilated Cardiomyopathy.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778334

Primary prevention of sudden death in patients with lamin A/C gene mutations.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778334

Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778334

A novel mutation, Ser143Pro, in the lamin A/C gene is common in finnish patients with familial dilated cardiomyopathy.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778334

Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778334

Brief report: deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778334

Severe Myocardial Fibrosis Caused by a Deletion of the 5’ End of the Lamin A/C Gene

18 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2012.276

High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2012.276

Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2012.276

Epidemiology of idiopathic dilated and hypertrophic cardiomyopathy. A population-based study in Olmsted County, Minnesota, 1975-1984

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23249954

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23249954

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Familial dilated cardiomyopathy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23249954

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/EJHG.2012.276

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Dimensions Publication ID

10 October 2017

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10 October 2017

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