Gain-of-Function Mutations in RIT1 Cause Noonan Syndrome, a RAS/MAPK Pathway Syndrome
- 20 June 2013
- journal article
- other
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 93 (1), 173-180
- https://doi.org/10.1016/j.ajhg.2013.05.021
Abstract
No abstract availableKeywords
Funding Information
- Ministry of Health, Labour and Welfare
- National Cancer Center (23-22-11)
- Japan Society for the Promotion of Science
- Ministry of Education, Culture, Sports, Science and Technology (LS004)
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