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

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Publication year
2021
Author(s)
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, 108, 11, (2021), pp. 2112-2129
ISSN
DOI
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/241137   https://hdl.handle.net/2066/241137
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