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Naslov Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome (Article)
Autori Capri Yline  ...  Cuturilo Goran  ...  (broj koautora 33) 
Info AMERICAN JOURNAL OF HUMAN GENETICS, (2019), vol. 104 br. 6, str. 1223-1232
Projekat ERN-ITHACA networking; E-Rare (NSEuroNet) [ERARE15-pp-063, 01GM1602B, 01GM1602A]; AIRC [IG21614]; Ministero della Salute; German Federal Ministry of Education and Research -BMBF (German Network for RASopathy Research "GeNeRARe") [01GM1519D, 01GM1902C, 01G
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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