Comprehensive mutation scanning of LMNA in 268 patients with lone atrial fibrillation (Q37230632)

19 August 2017

Comprehensive mutation scanning of LMNA in 268 patients with lone atrial fibrillation (English)

1 reference

19 August 2017

0 references

Katharine M Brauch

1

1 reference

19 August 2017

Lin Y Chen

series ordinal

2

1 reference

19 August 2017

Timothy M Olson

series ordinal

3

1 reference

19 August 2017

language of work or name

English

0 references

publication date

1 April 2009

1 reference

American Journal of Cardiology

19 August 2017

1 reference

19 August 2017

103

1 reference

19 August 2017

10

1 reference

19 August 2017

1426-1428

1 reference

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

19 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2697665

X-linked nonsyndromic sinus node dysfunction and atrial fibrillation caused by emerin mutation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2697665

The laminopathies: a clinical review

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2697665

Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2697665

Sodium channel mutations and susceptibility to heart failure and atrial fibrillation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2697665

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2697665

Mutations in the long QT gene, KCNQ1, are an uncommon cause of atrial fibrillation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2697665

Absence of TGFBR1 and TGFBR2 mutations in patients with bicuspid aortic valve and aortic dilation.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2697665

Cardiac sodium channel mutation in atrial fibrillation.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2697665

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

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2697665

Screening for mutations in a genetically heterogeneous disorder: DHPLC versus DNA sequence for mutation detection in multiple genes causing Charcot-Marie-Tooth neuropathy

4 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19427440

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19427440

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.AMJCARD.2009.01.354

1 reference

19 August 2017

1 reference

19 August 2017

1 reference