Phenotypes withGATA4 orNKX2.5 mutations in familial atrial septal defect-Reference-Cited by-同舟云学术

Phenotypes withGATA4 orNKX2.5 mutations in familial atrial septal defect

Published:2005 Issue:1 Volume:135A Page:47-52
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Hirayama-Yamada Kayoko,Kamisago Mitsuhiro,Akimoto Kaoru,Aotsuka Hiroyuki,Nakamura Yoshihide,Tomita Hideshi,Furutani Michiko,Imamura Shin-ichiro,Takao Atsuyoshi,Nakazawa Makoto,Matsuoka Rumiko

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference36 articles.

1. Mutations in human cause limb and cardiac malformation in Holt-Oram syndrome

2. Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations

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

4. A Murine Model of Holt-Oram Syndrome Defines Roles of the T-Box Transcription Factor Tbx5 in Cardiogenesis and Disease

5. The atrial natriuretic factor promoter is a downstream target for Nkx-2.5 in the myocardium

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