LHX2 haploinsufficiency causes a variable neurodevelopmental disorder
- Resource Type
- Article
- Authors
- 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