학술논문
LHX2 haploinsufficiency causes a variable neurodevelopmental disorder
Document Type
Article
Author
Schmid, Cosima M.; Gregor, Anne; Costain, Gregory; Morel, Chantal F.; Massingham, Lauren; Schwab, Jennifer; Quélin, Chloé; Faoucher, Marie; Kaplan, Julie; Procopio, Rebecca; Saunders, Carol J.; Cohen, Ana S.A.; Lemire, Gabrielle; Sacharow, Stephanie; O’Donnell-Luria, Anne; Segal, Ranit Jaron; Kianmahd Shamshoni, Jessica; Schweitzer, Daniela; Ebrahimi-Fakhari, Darius; Monaghan, Kristin; Palculict, Timothy Blake; Napier, Melanie P.; Tao, Alice; Isidor, Bertrand; Moradkhani, Kamran; Reis, André; Sticht, Heinrich; Chung, Wendy K.; Zweier, Christiane
Source
In Genetics in Medicine July 2023 25(7)
Subject
Language
ISSN
1098-3600