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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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Non-synonymous variants in pre-B cell leukemia homeobox (PBX) genes are associated with congenital heart defects

Cammon B Arrington1, Benjamin R Dowse, Steven B Bleyl

  • 1Department of Pediatrics, Division of Cardiology, University of Utah School of Medicine, Eccles Institute of Human Genetics, 15 North 2030 East, Room 7110B, Salt Lake City, UT 84112, USA.

European Journal of Medical Genetics
|March 20, 2012
PubMed

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