NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway.
McDaniell, Ryan; Warthen, Daniel M.; Sanchez-Lara, Pedro A.; Pai, Athma; Krantz, Ian D.; Piccoli, David A.; Spinner, Nancy B.; American Journal of Human Genetics, 2006, vol. 79, issue 1, p 169, ISSN 00029297. ISBN 00029297.

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