GATA5 loss-of-function mutation responsible for the congenital ventriculoseptal defect (Q43741626)

26 November 2017

title

GATA5 loss-of-function mutation responsible for the congenital ventriculoseptal defect (English)

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26 November 2017

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Dong Wei

1

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26 November 2017

Han Bao

2

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26 November 2017

Ning Zhou

3

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26 November 2017

Gui-Fen Zheng

4

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26 November 2017

Xing-Yuan Liu

5

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26 November 2017

Yi-Qing Yang

6

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26 November 2017

publication date

9 September 2012

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26 November 2017

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26 November 2017

volume

34

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26 November 2017

issue

3

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26 November 2017

page(s)

504-511

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Examining the cardiac NK-2 genes in early heart development.

26 November 2017

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Genetic screening of 104 patients with congenitally malformed hearts revealed a fresh mutation of GATA4 in those with atrial septal defects

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GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling

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GATA5 interacts with GATA4 and GATA6 in outflow tract development

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A novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect

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A novel GATA4 mutation completely segregated with atrial septal defect in a large Japanese family

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Spectrum of atrial septal defects associated with mutations of NKX2.5 and GATA4 transcription factors

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A novel GATA4 loss-of-function mutation associated with congenital ventricular septal defect.

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GATA4 mutations in 486 Chinese patients with congenital heart disease.

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Involvement of a novel GATA4 mutation in atrial septal defects

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12 December 2020

Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect

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12 December 2020

Mutational spectrum of the GATA5 gene associated with familial atrial fibrillation

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12 December 2020

Ventricular septal defects

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12 December 2020

Congenital Cardiac Defects: A Possible Association of Aminopterin Syndrome and In Utero Methotrexate Exposure?

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12 December 2020

A novel GATA6 mutation associated with congenital ventricular septal defect.

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12 December 2020

A novel GATA4 mutation responsible for congenital ventricular septal defects.

1 reference

12 December 2020

Brain Maturity and Brain Injury in Newborns With Cyanotic Congenital Heart Disease

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12 December 2020

Outcomes and Risk Factors for Mortality in Premature Neonates With Critical Congenital Heart Disease

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12 December 2020

A novel mutation of GATA4 in a familial atrial septal defect

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12 December 2020

Novel GATA4 mutations in patients with congenital ventricular septal defects.

1 reference

12 December 2020

10.1007/S00246-012-0482-6

Identifiers

DOI

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Dimensions Publication ID

26 November 2017

1031006213

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