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

Authors :: Motta, M.
Fasano, Giulia
Gredy, Sina
Brinkmann, Julia
Bonnard, Adeline Alice
Simsek-Kiper, P.O.
Boer, E. de
Vissers, L.E.L.M.
Zenker, M.
Tartaglia, M.
Motta, M.
Fasano, Giulia
Gredy, Sina
Brinkmann, Julia
Bonnard, Adeline Alice
Simsek-Kiper, P.O.
Boer, E. de
Vissers, L.E.L.M.
Zenker, M.
Tartaglia, M.
Source :: American Journal of Human Genetics; 2112; 2129; 0002-9297; 11; vol. 108; ~American Journal of Human Genetics~2112~2129~~~0002-9297~11~108~~
Publication Year :: 2021
Abstract: Item does not contain fulltext

Database :: OAIster
Journal :: American Journal of Human Genetics; 2112; 2129; 0002-9297; 11; vol. 108; ~American Journal of Human Genetics~2112~2129~~~0002-9297~11~108~~
Publication Type :: Electronic Resource
Accession number :: edsoai.on1290017977
Document Type :: Electronic Resource