Assessment of LMNA copy number variation in 58 probands with dilated cardiomyopathy (Q35492005)

8 August 2017

Assessment of LMNA copy number variation in 58 probands with dilated cardiomyopathy (English)

1 reference

8 August 2017

dilated cardiomyopathy

1 reference

Nadine Norton

1

1 reference

8 August 2017

Jill D Siegfried

series ordinal

2

1 reference

8 August 2017

Duanxiang Li

series ordinal

3

1 reference

8 August 2017

Ray E Hershberger

series ordinal

4

1 reference

8 August 2017

language of work or name

English

0 references

publication date

1 October 2011

1 reference

Clinical and Translational Science

8 August 2017

1 reference

8 August 2017

4

1 reference

8 August 2017

5

1 reference

8 August 2017

351-352

1 reference

Update 2011: clinical and genetic issues in familial dilated cardiomyopathy

8 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3205425

Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3205425

Identification of novel mutations in RBM20 in patients with dilated cardiomyopathy.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3205425

Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3205425

Genetic and ultrastructural studies in dilated cardiomyopathy patients: a large deletion in the lamin A/C gene is associated with cardiomyocyte nuclear envelope disruption

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3205425

Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3205425

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3205425

Mutations of presenilin genes in dilated cardiomyopathy and heart failure

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3205425

Identification of disease genes by whole genome CGH arrays

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3205425

DNA structural variants as genetic risk factors for the long QT syndrome

12 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22029807

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1111/J.1752-8062.2011.00305.X

1 reference

8 August 2017

1 reference

8 August 2017

1 reference