NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway
University of Pennsylvania · Children's Hospital of Philadelphia
Indexed incrossrefpubmed
Abstract
No abstract available for this paper.
Citation impact
743
total citations
- FWCI
- 28.22
- Percentile
- 100%
- References
- 24
Citations per year
Authors
7- RMRyan M. McDaniell
University of Pennsylvania, Children's Hospital of Philadelphia
- DMDaniel M. Warthen
University of Pennsylvania, Children's Hospital of Philadelphia
- PAPedro A. Sanchez‐Lara
University of Pennsylvania, Children's Hospital of Philadelphia
- AAAthma A. Pai
University of Pennsylvania, Children's Hospital of Philadelphia
- IDIan D. Krantz
Children's Hospital of Philadelphia, University of Pennsylvania
Topics & keywords
Topics
Keywords
- Alagille syndrome
- Notch signaling pathway
- Medicine
- Genetics
- Biology
- Cancer research
- Signal transduction
- Internal medicine
UN Sustainable Development Goals
- Good health and well-being
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