Apical left ventricular aneurysm without atrio-ventricular block due to a lamin A/C gene mutation-Reference-Cited by-同舟云学术

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

Published:2003-12 Issue:6 Volume:5 Page:821-825
ISSN:1388-9842
Container-title:European Journal of Heart Failure
language:en
Short-container-title:European Journal of Heart Failure

Author:

Forissier Jean-François¹²,Bonne Gisèle³⁴,Bouchier Christiane⁴⁵,Duboscq-Bidot Laetitia⁴⁵,Richard Pascale⁴⁶,Wisnewski Claudine³⁴,Briault Sylvain⁷,Moraine Claude⁷,Dubourg Olivier¹,Schwartz Ketty³⁴,Komajda Michel⁴⁵⁸

Affiliation:

1. Service de Cardiologie; Hôpital Ambroise Paré; Boulogne-Billancourt France

2. Centre cardiologique Arago; Perpignan France

3. Inserm U582, Institut de Myologie; Groupe Hospitalier Pitié-Salpêtrière; Paris France

4. IFR 14 Cœur, Muscles et Vaisseaux; Groupe Hospitalier Pitié-Salpêtrière; Paris France

5. Laboratoire Génétique et Insuffisance Cardiaque; Association Claude Bernard/Université Paris VI, Groupe Hospitalier Pitié-Salpêtrière; Paris France

6. Service de Biochimie B; Groupe Hospitalier Pitié-Salpêtrière; Paris France

7. Service de Génétique; Hôpital Bretonneau; Tours France

8. Service de Cardiologie; Groupe Hospitalier Pitié-Salpêtrière; Paris France

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

Reference21 articles.

1. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy;Bonne;Nature Genet,1999

2. Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B);Muchir;Hum Mol Genet,2000

3. High incidence of sudden death of conduction system and myocardial disease due to lamins A/C gene mutation;Bécane;Pacing Clin Electrophysiol,2000

4. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease;Fatkin;N Engl J Med,1999

5. LMNA, encoding lamin A/C, is mutated in partial lipodystrophy;Shackleton;Nature Genet,2000

Cited by 38 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The Pathogenic Mechanisms of and Novel Therapies for Lamin A/C-Related Dilated Cardiomyopathy Based on Patient-Specific Pluripotent Stem Cell Platforms and Animal Models;Pharmaceuticals;2024-08-05

2. The LMNA p.R541C mutation causes dilated cardiomyopathy in human and mice;International Journal of Cardiology;2022-09

3. Clinical and Genomic Evaluation of 207 Genetic Myopathies in the Indian Subcontinent;Frontiers in Neurology;2020-11-05

4. Clinical and Genomic Evaluation of 207 Genetic Myopathies in the Indian Subcontinent;2020-09-18

5. Genotype–phenotype correlation of LMNA variants involving the Arg541 residue: a case report with multimodality imaging and literature review;ESC Heart Failure;2020-07-15