Noonan syndrome gain-of-function mutations in NRAS cause zebrafish gastrulation defects
SUMMARY Noonan syndrome is a relatively common developmental disorder that is characterized by reduced growth, wide-set eyes and congenital heart defects. Noonan syndrome is associated with dysregulation of the Ras–mitogen-activated-protein-kinase (MAPK) signaling pathway. Recently, two mutations in...
Main Authors: | , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
The Company of Biologists
2011-05-01
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Series: | Disease Models & Mechanisms |
Online Access: | http://dmm.biologists.org/content/4/3/393 |