(Q34195576)

31 July 2017

title

Recurrent and founder mutations in the Netherlands: mutation p.K217del in troponin T2, causing dilated cardiomyopathy (English)

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31 July 2017

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E Otten

1

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31 July 2017

R H Lekanne Dit Deprez

2

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31 July 2017

M M Weiss

3

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31 July 2017

M van Slegtenhorst

4

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31 July 2017

M Joosten

5

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31 July 2017

J J van der Smagt

6

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31 July 2017

N de Jonge

7

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31 July 2017

W S Kerstjens-Frederikse

8

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31 July 2017

M T R Roofthooft

9

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31 July 2017

A H M M Balk

10

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31 July 2017

M P van den Berg

11

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31 July 2017

J S Ruiter

12

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31 July 2017

J P van Tintelen

13

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31 July 2017

publication date

1 October 2010

1 reference

Netherlands Heart Journal

31 July 2017

published in

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31 July 2017

volume

18

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31 July 2017

issue

10

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31 July 2017

page(s)

478-485

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https://scigraph.springernature.com/pub.10.1007/bf03091819

31 July 2017

exact match

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cites work

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Registry of the International Society for Heart and Lung Transplantation: Twenty-sixth Official Adult Heart Transplant Report-2009.

5 July 2018

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

5 July 2018

1 reference

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5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954300

Cardiac troponin T mutation in familial cardiomyopathy with variable remodeling and restrictive physiology

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954300

Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy

5 July 2018

1 reference

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Mutations in sarcomere protein genes in left ventricular noncompaction

5 July 2018

1 reference

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Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes

5 July 2018

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DNA analysis in inherited cardiomyopathies: current status and clinical relevance

5 July 2018

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Inherited cardiomyopathies as a troponin disease

5 July 2018

1 reference

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Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954300

Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy

5 July 2018

1 reference

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Alterations in thin filament regulation induced by a human cardiac troponin T mutant that causes dilated cardiomyopathy are distinct from those induced by troponin T mutants that cause hypertrophic cardiomyopathy

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954300

Cardiac troponin T lysine 210 deletion in a family with dilated cardiomyopathy

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954300

Ca(2+)-desensitizing effect of a deletion mutation Delta K210 in cardiac troponin T that causes familial dilated cardiomyopathy.

5 July 2018

1 reference

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Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy

5 July 2018

1 reference

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The Genetic Basis for Cardiomyopathy

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954300

Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954300

Isolated noncompaction of the myocardium in adults

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954300

Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases.

5 July 2018

1 reference

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Familial dilated cardiomyopathy with troponin T K210del mutation.

28 October 2018

1 reference

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28 October 2018

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Two novel mutations in the beta-myosin heavy chain gene associated with dilated cardiomyopathy

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954300

Novel troponin T mutation in familial dilated cardiomyopathy with gender-dependant severity

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954300

Novel mutations in sarcomeric protein genes in dilated cardiomyopathy.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954300

The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954300

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

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954300

Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954300

Natural history of dilated cardiomyopathy due to lamin A/C gene mutations

28 October 2018

1 reference

12 December 2020

Large-scale mutation screening in patients with dilated or hypertrophic cardiomyopathy: a pilot study using DGGE

1 reference

12 December 2020

Gene mutations in adult Japanese patients with dilated cardiomyopathy

1 reference

12 December 2020

Different functional properties of troponin T mutants that cause dilated cardiomyopathy

1 reference

12 December 2020

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF03091819

1 reference

Dimensions Publication ID

31 July 2017

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1 reference

31 July 2017

1 reference