Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome
- 5 June 2019
- journal article
- research article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 104 (6), 1223-1232
- https://doi.org/10.1016/j.ajhg.2019.04.013
Abstract
No abstract availableFunding Information
- Associazione Italiana per la Ricerca sul Cancro
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