학술논문
LHX2 haploinsufficiency causes a variable neurodevelopmental disorder
Document Type
Article
Author
Schmid, C.M.; Gregor, A.; Zweier, C.; Costain, G.; Morel, C.F.; Massingham, L.; Schwab, J.; Quélin, C.; Faoucher, M.; Kaplan, J.; Procopio, R.; Saunders, C.J.; Cohen, A.S.A.; Lemire, G.; O'Donnell-Luria, A.; Sacharow, S.; Segal, R.J.; Kianmahd Shamshoni, J.; Schweitzer, D.; Ebrahimi-Fakhari, D.; Monaghan, K.; Palculict, T.B.; Napier, M.P.; Tao, A.; Isidor, B.; Moradkhani, K.; Reis, A.; Sticht, H.; Chung, W.K.
Source
In: Genetics in Medicine . (Genetics in Medicine, July 2023, 25(7))
Subject
Language
English
ISSN
15300366
10983600
10983600