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2006•The American Journal of Human GeneticsOpen access

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

Ryan M. McDaniell, Daniel M. Warthen, Pedro Alfonso Sanchez-Lara, Athma A. Pai, Ian D. Krantz, David A. Piccoli, Nancy Bettina Spinner

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Key concepts: Alagille syndrome, Notch signaling pathway, Medicine, Genetics, Biology, Cancer research, Signal transduction, Internal medicine

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NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway — Research Paper | ScholarLens