Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome-Reference-Cited by-同舟云学术

Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome

Published:2019-06 Issue:6 Volume:104 Page:1223-1232
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Capri Yline,Flex Elisabetta,Krumbach Oliver H.F.,Carpentieri Giovanna,Cecchetti Serena,Lißewski Christina,Rezaei Adariani Soheila,Schanze Denny,Brinkmann Julia,Piard Juliette,Pantaleoni Francesca,Lepri Francesca R.,Goh Elaine Suk-Ying,Chong Karen,Stieglitz Elliot,Meyer Julia,Kuechler Alma,Bramswig Nuria C.,Sacharow Stephanie,Strullu Marion,Vial Yoann,Vignal Cédric,Kensah George,Cuturilo Goran,Kazemein Jasemi Neda S.,Dvorsky Radovan,Monaghan Kristin G.,Vincent Lisa M.,Cavé Hélène,Verloes Alain,Ahmadian Mohammad R.,Tartaglia Marco,Zenker Martin

Funder

E-Rare

AIRC

Ministero della Salute

German Federal Ministry of Education and Research - BMBF

German Research Foundation

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference56 articles.

1. Noonan syndrome;Roberts;Lancet,2013