(Q42827539)

8 November 2017

Miscues on the "lack of MEF2A mutations" in coronary artery disease (English)

1 reference

8 November 2017

3

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8 November 2017

Shaoqi Rao

2

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author name string

Qing Wang

series ordinal

1

1 reference

PMC publication ID

1137019

8 November 2017

language of work or name

English

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publication date

1 June 2005

1 reference

Journal of Clinical Investigation

8 November 2017

1 reference

8 November 2017

115

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8 November 2017

6

1 reference

8 November 2017

1399-400; author reply 1400-1

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Lack of MEF2A mutations in coronary artery disease

8 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1137019

MEF2A sequence variants and coronary artery disease: a change of heart?

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1137019

Transcription factor MEF2A mutations in patients with coronary artery disease

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1137019

Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genomewide linkage analysis

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1137019

Mutation of MEF2A in an inherited disorder with features of coronary artery disease

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1137019

SNP S1103Y in the cardiac sodium channel gene SCN5A is associated with cardiac arrhythmias and sudden death in a white family

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1137019

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1137019

Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1137019

Distinct domains of myocyte enhancer binding factor-2A determining nuclear localization and cell type-specific transcriptional activity

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1137019

27 May 2018

Identifiers

DOI

10.1172/JCI25475

1 reference

8 November 2017

1 reference

PMC publication ID

1137019

8 November 2017

PubMed publication ID

15931371

1 reference

PMC publication ID

1137019