| Title: | Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome |
Authors: | 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; Čuturilo, Goran   ; Kazemein, Jasemi Neda S.; Dvorsky, Radovan; Monaghan, Kristin G.; Vincent, Lisa M.; Cavé, Hélène; Verloes, Alain; Ahmadian, Mohammad R.; Tartaglia, Marco; Zenker, Martin;
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Issue Date: | 2019 |
Publication: | The American Journal of Human Genetics |
ISSN: | 0002-9297 American Journal of Human Genetics Search Idenfier |
Type: | Article |
Collation: | vol. 104 br. 6 str. 1223-1232 |
DOI: | 10.1016/j.ajhg.2019.04.013 |
WoS-ID: | 000470240000016 |
Scopus-ID: | 2-s2.0-85066434161 |
PMID: | 31130282 |
PMCID: | PMC6562003 |
URI: | https://enauka.gov.rs/handle/123456789/222061 |
Metadata source: | Migrirano iz RIS podataka |
M-category: | |