The role of Lamin A/C mutations in Danish patients with idiopathic dilated cardiomyopathy (Q50550233)

15 March 2018

title

The role of Lamin A/C mutations in Danish patients with idiopathic dilated cardiomyopathy (English)

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author

Finn Gustafsson

3

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Paula Louise Hedley

4

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Henning Bundgaard

6

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Christian Torp-Pedersen

8

object named as

Christian Torp-Pedersen

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9

Lars Køber

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10

Michael Christiansen

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author name string

Daniel Vega Møller

1

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Tam Thanh Pham

2

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Mads Kristian Ersbøll

5

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Claus B Andersen

7

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publication date

1 November 2009

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European Journal of Heart Failure

published in

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volume

11

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issue

11

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page(s)

1031-1035

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Genetics of dilated cardiomyopathy

cites work

1 reference

https://api.crossref.org/works/10.1093%2FEURJHF%2FHFP134

Genetic causes of human heart failure

21 January 2018

1 reference

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Genetic and phenotypic analysis of dilated cardiomyopathy with conduction system disease: demand for strategies in the management of presymptomatic lamin A/C mutant carriers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURJHF%2FHFP134

Both lamin A and lamin C mutations cause lamina instability as well as loss of internal nuclear lamin organization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURJHF%2FHFP134

A-type lamins: guardians of the soma?

21 January 2018

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https://api.crossref.org/works/10.1093%2FEURJHF%2FHFP134

A novel role for the nuclear membrane protein emerin in association of the centrosome to the outer nuclear membrane

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURJHF%2FHFP134

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURJHF%2FHFP134

Incomplete nonsense-mediated decay of mutant lamin A/C mRNA provokes dilated cardiomyopathy and ventricular tachycardia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURJHF%2FHFP134

Phenotypic clustering of lamin A/C mutations in neuromuscular patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURJHF%2FHFP134

LMNA mutations in cardiac transplant recipients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURJHF%2FHFP134

Extreme variability of skeletal and cardiac muscle involvement in patients with mutations in exon 11 of the lamin A/C gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURJHF%2FHFP134

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURJHF%2FHFP134

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURJHF%2FHFP134

Long-Term Outcome and Risk Stratification in Dilated Cardiolaminopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURJHF%2FHFP134

Extreme phenotypic diversity and nonpenetrance in families with theLMNA gene mutation R644C

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURJHF%2FHFP134

21 January 2018

Identifiers

DOI

10.1093/EURJHF/HFP134

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15 March 2018