Notch signaling in human development and disease.
Penton AL, Leonard LD, Spinner NB.
Penton AL, et al.
Semin Cell Dev Biol. 2012 Jun;23(4):450-7. doi: 10.1016/j.semcdb.2012.01.010. Epub 2012 Jan 28.
Semin Cell Dev Biol. 2012.
PMID: 22306179
Free PMC article.
Review.
Notch associated disorders include the autosomal dominant, multi-system, Alagille syndrome caused by mutations in both a ligand (Jagged1 (JAG1)) and receptor (NOTCH2) and autosomal recessive spondylocostal dysostosis, caused by mutations in a li …
Notch associated disorders include the autosomal dominant, multi-system, Alagille syndrome caused by mutations in both a ligand (Jagg …