Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia-Reference-Cited by-同舟云学术

Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia

Published:2012-11-09 Issue:3 Volume:132 Page:285-292
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Yu Lan,Wynn Julia,Cheung Yee Him,Shen Yufeng,Mychaliska George B.,Crombleholme Timothy M.,Azarow Kenneth S.,Lim Foong Yen,Chung Dai H.,Potoka Douglas,Warner Brad W.,Bucher Brian,Stolar Charles,Aspelund Gudrun,Arkovitz Marc S.,Chung Wendy K.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-012-1249-0.pdf

Reference29 articles.

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2. Adzhubei IA, Schmidt S, Peshkin L, Ramensky VE, Gerasimova A, Bork P, Kondrashov AS, Sunyaev SR (2010) A method and server for predicting damaging missense mutations. Nat Methods 7:248–249

3. Arceci RJ, King AA, Simon MC, Orkin SH, Wilson DB (1993) Mouse GATA-4: a retinoic acid-inducible GATA-binding transcription factor expressed in endodermally derived tissues and heart. Mol Cell Biol 13:2235–2246

4. Bouchard MF, Taniguchi H, Viger RS (2009) The effect of human GATA4 gene mutations on the activity of target gonadal promoters. J Mol Endocrinol 42:149–160

5. Brady PD, Srisupundit K, Devriendt K, Fryns JP, Deprest JA, Vermeesch JR (2011) Recent developments in the genetic factors underlying congenital diaphragmatic hernia. Fetal Diagn Ther 29:25–39

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