(Q33493228)

27 July 2017

title

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

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27 July 2017

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Hirotomo Saitsu

7

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author name string

Haruka Hamanoue

1

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27 July 2017

Sri Endah Rahayuningsih

2

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27 July 2017

Yuya Hirahara

3

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27 July 2017

Junko Itoh

4

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27 July 2017

Utako Yokoyama

5

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27 July 2017

Takeshi Mizuguchi

6

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27 July 2017

Noriko Miyake

8

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27 July 2017

Fumiki Hirahara

9

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27 July 2017

Naomichi Matsumoto

10

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27 July 2017

publication date

13 August 2009

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27 July 2017

published in

Cardiology in the Young

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27 July 2017

volume

19

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27 July 2017

issue

5

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27 July 2017

page(s)

482-485

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

27 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109990813

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109990813

The incidence of congenital heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109990813

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109990813

Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109990813

Functional analyses of three Csx/Nkx-2.5 mutations that cause human congenital heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109990813

GATA4 mutations in 486 Chinese patients with congenital heart disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109990813

Novel point mutation in the cardiac transcription factor CSX/NKX2.5 associated with congenital heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109990813

Two novel frameshift mutations in NKX2.5 result in novel features including visceral inversus and sinus venosus type ASD

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109990813

Novel NKX2-5 mutations in diseased heart tissues of patients with cardiac malformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109990813

A novel mutation in the GATA4 gene in patients with Tetralogy of Fallot.

21 January 2018

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https://api.crossref.org/works/10.1017%2FS1047951109990813

NKX2.5 mutations in patients with tetralogy of fallot

21 January 2018

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https://api.crossref.org/works/10.1017%2FS1047951109990813

21 January 2018

https://api.crossref.org/works/10.1017%2FS1047951109990813

7 January 2021

Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109990813

Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109990813

Spectrum of heart disease associated with murine and human GATA4 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109990813

Congenital heart disease caused by mutations in the transcription factor NKX2-5

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109990813

GATA4 sequence variants in patients with congenital heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109990813

Cardiac transcription factor Csx/Nkx2-5: Its role in cardiac development and diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109990813

GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109990813

Screening and biochemical analysis of GATA4 sequence variations identified in patients with congenital heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109990813

7 January 2021

NKX2.5mutations in patients with congenital heart disease

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109990813

7 January 2021

We need a detailed phenome in the phenomenon of genetics and congenital heart disease

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109990813

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109990813

7 January 2021

10.1017/S1047951109990813

Identifiers

DOI

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27 July 2017

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