(Q35954331)

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Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death?

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Europe PubMed Central

PubMed publication ID

11 August 2017

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Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death? (English)

1 reference

Europe PubMed Central

PubMed publication ID

11 August 2017

1 reference

based on heuristic

inferred from title

Harry J. G. M. Crijns

11

object named as

Harry J G M Crijns

1 reference

Europe PubMed Central

PubMed publication ID

11 August 2017

Anneke J van der Kooi

3

object named as

Anneke J van der Kooi

1 reference

Europe PubMed Central

PubMed publication ID

11 August 2017

Marianne de Visser

10

object named as

Marianne de Visser

1 reference

Europe PubMed Central

PubMed publication ID

11 August 2017

author name string

Jop H van Berlo

1

1 reference

Europe PubMed Central

PubMed publication ID

11 August 2017

Willem G de Voogt

2

1 reference

Europe PubMed Central

PubMed publication ID

11 August 2017

J Peter van Tintelen

4

1 reference

Europe PubMed Central

PubMed publication ID

11 August 2017

Gisèle Bonne

5

1 reference

Europe PubMed Central

PubMed publication ID

11 August 2017

Rabah Ben Yaou

6

1 reference

Europe PubMed Central

PubMed publication ID

11 August 2017

Denis Duboc

7

1 reference

Europe PubMed Central

PubMed publication ID

11 August 2017

Tom Rossenbacker

8

1 reference

Europe PubMed Central

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11 August 2017

Hein Heidbüchel

9

1 reference

Europe PubMed Central

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11 August 2017

Yigal M Pinto

12

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11 August 2017

publication date

13 November 2004

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Europe PubMed Central

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11 August 2017

Journal of Molecular Medicine

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Europe PubMed Central

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11 August 2017

83

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Europe PubMed Central

PubMed publication ID

11 August 2017

1

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11 August 2017

79-83

1 reference

Europe PubMed Central

PubMed publication ID

11 August 2017

A missense mutation in the exon 8 of lamin A/C gene in a Japanese case of autosomal dominant limb-girdle muscular dystrophy and cardiac conduction block

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifuss muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The nuclear envelope lamina is reversibly depolymerized during mitosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant Emery-Dreifuss dystrophy due to mutations in rod domain of the lamin A/C gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation analysis of the lamin A/C gene (LMNA) among patients with different cardiomuscular phenotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Skeletal muscle pathology in autosomal dominant Emery-Dreifuss muscular dystrophy with lamin A/C mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

cDNA sequencing of nuclear lamins A and C reveals primary and secondary structural homology to intermediate filament proteins

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvement

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homologies in both primary and secondary structure between nuclear envelope and intermediate filament proteins

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new frameshift mutation at codon 466 (1397delA) within the LMNA gene.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Emery-Dreifuss muscular dystrophy: disease spectrum and differential diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Out-of-hospital cardiac arrest in the 1990's: a population-based study in the Maastricht area on incidence, characteristics and survival

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early and severe presentation of autosomal dominant Emery-Dreifuss muscular dystrophy (EMD2)

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant Emery-Dreifuss muscular dystrophy: a new family with late diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic localization of a newly recognized autosomal dominant limb-girdle muscular dystrophy with cardiac involvement (LGMD1B) to chromosome 1q11-21.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Genetic Basis for Cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551023

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00109-004-0589-1

1 reference

Europe PubMed Central

PubMed publication ID

11 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

11 August 2017

ResearchGate publication ID

0 references

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