학술논문
Neurodevelopmental and other phenotypes recurrently associated with heterozygous BAZ2B loss-of-function variants
Document Type
Article
Author
Sewani, S.; Azamian, M.S.; Zhao, X.; Lalani, S.R.; Scott, D.A.; Mendelsohn, B.A.; Mau-Them, F.T.; Réda, M.; Nambot, S.; Isidor, B.; van der Smagt, J.J.; Shen, J.J.; Shillington, A.; White, L.; Elloumi, H.Z.; Baker, P.R.; Svihovec, S.; Brown, K.; Koopman-Keemink, Y.; Hoffer, M.J.V.; Lakeman, I.M.M.; Brischoux-Boucher, E.; Kinali, M.
Source
In: American Journal of Medical Genetics, Part A . (American Journal of Medical Genetics, Part A, March 2024, 194(3))
Subject
Language
English
ISSN
15524833
15524825
15524825