SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype-Reference-Cited by-同舟云学术

SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype

Published:2021-11 Issue:11 Volume:108 Page:2112-2129
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Motta Marialetizia,Fasano Giulia,Gredy Sina,Brinkmann Julia,Bonnard Adeline Alice,Simsek-Kiper Pelin Ozlem,Gulec Elif Yilmaz,Essaddam Leila,Utine Gulen Eda,Guarnetti Prandi Ingrid,Venditti Martina,Pantaleoni Francesca,Radio Francesca Clementina,Ciolfi Andrea,Petrini Stefania,Consoli Federica,Vignal Cédric,Hepbasli Denis,Ullrich Melanie,de Boer Elke,Vissers Lisenka E.L.M.,Gritli Sami,Rossi Cesare,De Luca Alessandro,Ben Becher Saayda,Gelb Bruce D.,Dallapiccola Bruno,Lauri Antonella,Chillemi Giovanni,Schuh Kai,Cavé Hélène,Zenker Martin,Tartaglia Marco^ORCID

Funder

German Research Foundation

Associazione Italiana per la Ricerca sul Cancro

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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