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

✍ Scribed by Ryan McDaniell; Daniel M. Warthen; Pedro A. Sanchez-Lara; Athma Pai; Ian D. Krantz; David A. Piccoli; Nancy B. Spinner


Book ID
117854844
Publisher
American Society of Human Genetics
Year
2006
Tongue
English
Weight
998 KB
Volume
79
Category
Article
ISSN
0002-9297

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