A novel autosomal dominant condition consisting of congenital heart defects and low atrial rhythm maps to chromosome 9q-Reference-Cited by-同舟云学术

A novel autosomal dominant condition consisting of congenital heart defects and low atrial rhythm maps to chromosome 9q

Published:2011-03-09 Issue:7 Volume:19 Page:820-826
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

van de Meerakker Judith B A,van Engelen Klaartje,Mathijssen Inge B,Lekanne dit Deprez Ronald H,Lam Jan,Wilde Arthur A M,Baars Marieke J H,Mannens Marcel M A M,Mulder Barbara J M,Moorman Antoon F M,Postma Alex V

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/ejhg201133.pdf

Reference27 articles.

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2. Schott JJ, Benson DW, Basson CT et al: Congenital heart disease caused by mutations in the transcription factor NKX2-5. Science 1998; 281: 108–111.

3. Garg V, Kathiriya IS, Barnes R et al: GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5. Nature 2003; 424: 443–447.

4. Benson DW, Sharkey A, Fatkin D et al: Reduced penetrance, variable expressivity, and genetic heterogeneity of familial atrial septal defects. Circulation 1998; 97: 2043–2048.

5. Garg V, Muth AN, Ransom JF et al: Mutations in NOTCH1 cause aortic valve disease. Nature 2005; 437: 270–274.

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