학술논문
ATP2B2 de novo variants as a cause of variable neurodevelopmental disorders that feature dystonia, ataxia, intellectual disability, behavioral symptoms, and seizures
Document Type
Article
Author
Poggio, E.; Salmaso, A.; Milani, C.; Brini, M.; Barazzuol, L.; Deligiannopoulou, A.; Calì, T.; Cazorla, Á.G.; Jang, S.S.; Juliá-Palacios, N.; Keren, B.; Mignot, C.; Kopajtich, R.; Neuhofer, C.; Prokisch, H.; Winkelmann, J.; Zech, M.; Lynch, S.A.; Moorwood, C.; Nigro, V.; Torella, A.; Oostra, A.; Saillour, V.; Schuermans, N.; Verloo, P.; Yazbeck, E.; Zollino, M.; Jech, R.; Necpal, J.
Source
In: Genetics in Medicine . (Genetics in Medicine, December 2023, 25(12))
Subject
Language
English
ISSN
15300366
10983600
10983600