๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Corrigendum: Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome

โœ Scribed by Tartaglia, Marco; Pennacchio, Len A; Zhao, Chen; Yadav, Kamlesh K; Fodale, Valentina; Sarkozy, Anna; Pandit, Bhaswati; Oishi, Kimihiko; Martinelli, Simone; Schackwitz, Wendy


Book ID
109915088
Publisher
Nature Publishing Group
Year
2007
Tongue
English
Weight
78 KB
Volume
39
Category
Article
ISSN
1061-4036

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Gain-of-function RAF1 mutations cause No
โœ Pandit, Bhaswati; Sarkozy, Anna; Pennacchio, Len A; Carta, Claudio; Oishi, Kimih ๐Ÿ“‚ Article ๐Ÿ“… 2007 ๐Ÿ› Nature Publishing Group ๐ŸŒ English โš– 224 KB

Noonan and LEOPARD syndromes are developmental disorders with overlapping features, including cardiac abnormalities, short stature and facial dysmorphia. Increased RAS signaling owing to PTPN11, SOS1 and KRAS mutations causes B60% of Noonan syndrome cases , and PTPN11 mutations cause 90% of LEOPARD