KLF13 is a genetic modifier of the Holt-Oram syndrome gene TBX5-Reference-Cited by-同舟云学术

KLF13 is a genetic modifier of the Holt-Oram syndrome gene TBX5

Published:2017-01-09 Issue:5 Volume:26 Page:942-954
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Darwich Rami¹,Li Wenjuan¹²,Yamak Abir¹,Komati Hiba¹,Andelfinger Gregor³,Sun Kun²,Nemer Mona¹

Affiliation:

1. Molecular Genetics and Cardiac Regeneration Laboratory, Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, K1N 6N5, Canada

2. Department of Pediatric Cardiology, Xinhua Hospital, Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, People’s Republic of China

3. Sainte Justine Hospital, Cardiovascular Genetics, Montréal, Quebec, H3T 1C5, Canada

Funder

the Heart and Stroke Foundation of Canada

Canadian Institute for Health Research

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/26/5/942/11144484/ddx009.pdf

Reference35 articles.

1. Genetics of congenital heart disease: the glass half empty;Fahed;Circ. Res,2013