ISSN:
1546-1718
Source:
Nature Archives 1869 - 2009
Topics:
Biology
,
Medicine
Notes:
[Auszug] Noonan syndrome is characterized by short stature, facial dysmorphia and a wide spectrum of congenital heart defects. Mutations of PTPN11, KRAS and SOS1 in the RAS-MAPK pathway cause ∼60% of cases of Noonan syndrome. However, the gene(s) responsible for the remainder are unknown. We have ...
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1038/ng2078
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