NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway

Ryan M. McDaniell(University of Pennsylvania), Daniel M. Warthen(University of Pennsylvania), Pedro A. Sanchez‐Lara(University of Pennsylvania), Athma A. Pai(University of Pennsylvania), Ian D. Krantz(Children's Hospital of Philadelphia), David A. Piccoli(Children's Hospital of Philadelphia), Nancy B. Spinner(Children's Hospital of Philadelphia)
The American Journal of Human Genetics
June 7, 2006
10.1086/505332
Cited by 743Open Access
Full Text

Abstract

Related Papers

No related papers found

Powered by citation graph analysis