(Q63531445)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14675861%20AND%20SRC:MED&resulttype=core&format=json

22 December 2019

title

Apical left ventricular aneurysm without atrio-ventricular block due to a lamin A/C gene mutation (English)

1 reference

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22 December 2019

1 reference

2

1 reference

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22 December 2019

11

Michel Komajda

1 reference

22 December 2019

author name string

Jean-François Forissier

1

1 reference

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22 December 2019

Christiane Bouchier

3

1 reference

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22 December 2019

Laetitia Duboscq-Bidot

4

1 reference

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22 December 2019

Pascale Richard

5

1 reference

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22 December 2019

Claudine Wisnewski

6

1 reference

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22 December 2019

Sylvain Briault

7

1 reference

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22 December 2019

Claude Moraine

8

1 reference

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22 December 2019

Olivier Dubourg

9

1 reference

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22 December 2019

Ketty Schwartz

10

1 reference

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22 December 2019

publication date

1 December 2003

1 reference

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European Journal of Heart Failure

22 December 2019

published in

1 reference

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22 December 2019

volume

5

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22 December 2019

issue

6

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22 December 2019

page(s)

821-825

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Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

22 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1388-9842%2803%2900149-1

7 January 2021

Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)

1 reference

https://api.crossref.org/works/10.1016%2FS1388-9842%2803%2900149-1

7 January 2021

High Incidence of Sudden Death with Conduction System and Myocardial Disease Due to Lamins A and C Gene Mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1388-9842%2803%2900149-1

7 January 2021

Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease

1 reference

https://api.crossref.org/works/10.1016%2FS1388-9842%2803%2900149-1

7 January 2021

LMNA, encoding lamin A/C, is mutated in partial lipodystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS1388-9842%2803%2900149-1

7 January 2021

Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C

1 reference

https://api.crossref.org/works/10.1016%2FS1388-9842%2803%2900149-1

7 January 2021

Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse

1 reference

https://api.crossref.org/works/10.1016%2FS1388-9842%2803%2900149-1

7 January 2021

Lamin a truncation in Hutchinson-Gilford progeria.

1 reference

https://api.crossref.org/works/10.1016%2FS1388-9842%2803%2900149-1

7 January 2021

Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS1388-9842%2803%2900149-1

7 January 2021

Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene

1 reference

https://api.crossref.org/works/10.1016%2FS1388-9842%2803%2900149-1

7 January 2021

Lamin A/C Gene Mutation Associated With Dilated Cardiomyopathy With Variable Skeletal Muscle Involvement

1 reference

https://api.crossref.org/works/10.1016%2FS1388-9842%2803%2900149-1

7 January 2021

Distinguishing left ventricular aneurysm from pseudoaneurysm. A review of the literature

1 reference

https://api.crossref.org/works/10.1016%2FS1388-9842%2803%2900149-1

7 January 2021

Left ventricular pseudoaneurysm.

1 reference

https://api.crossref.org/works/10.1016%2FS1388-9842%2803%2900149-1

7 January 2021

Left ventricular pseudoaneurysm complicating infective pericarditis

1 reference

https://api.crossref.org/works/10.1016%2FS1388-9842%2803%2900149-1

7 January 2021

Apical left ventricular aneurysms and cardiac parasympathetic innervation in Chagas' heart disease

1 reference

https://api.crossref.org/works/10.1016%2FS1388-9842%2803%2900149-1

7 January 2021

Hypertrophic cardiomyopathy with apical left ventricular aneurysm

1 reference

https://api.crossref.org/works/10.1016%2FS1388-9842%2803%2900149-1

7 January 2021

A R644C mutation within lamin A extends the mutations causing dilated cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS1388-9842%2803%2900149-1

7 January 2021

Mutations in the LMNA gene encoding lamin A/C

1 reference

https://api.crossref.org/works/10.1016%2FS1388-9842%2803%2900149-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1388-9842%2803%2900149-1

7 January 2021

The Ig-like structure of the C-terminal domain of lamin A/C, mutated in muscular dystrophies, cardiomyopathy, and partial lipodystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS1388-9842%2803%2900149-1

7 January 2021

10.1016/S1388-9842(03)00149-1

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14675861%20AND%20SRC:MED&resulttype=core&format=json

22 December 2019

1 reference