학술논문
EIF3F-related neurodevelopmental disorder: refining the phenotypic and expanding the molecular spectrum
Document Type
Article
Author
Hüffmeier, U.; Kraus, C.; Reuter, M.S.; Uebe, S.; Schuhmann, S.; Reis, A.; Zweier, C.; Abbott, M.-A.; Ahmed, S.A.; Rawson, K.L.; Barr, E.; Li, H.; Bruel, A.-L.; Faivre, L.; Tran Mau-Them, F.; Botti, C.; Brooks, S.; Burns, K.; Ward, D.I.; Dutra-Clarke, M.; Martinez-Agosto, J.A.; Nelson, S.F.; Lee, H.; Zacher, P.; Abou Jamra, R.; Klöckner, C.; McGaughran, J.; Kohlhase, J.; Moran, E.; Pappas, J.; Raas-Rothschild, A.; Sacoto, M.J.G.; Henderson, L.B.; Palculict, T.B.; Mullegama, S.V.; Zghal Elloumi, H.; Reich, A.; Schrier Vergano, S.A.; Wahl, E.
Source
In: Orphanet Journal of Rare Diseases . (Orphanet Journal of Rare Diseases, December 2021, 16(1))
Subject
Language
English
ISSN
17501172