학술논문
Haploinsufficiency of the Sin3/HDAC corepressor complex member SIN3B causes a syndromic intellectual disability/autism spectrum disorder
Document Type
Article
Author
Latypova, X.; Vincent, M.; Le Caignec, C.; Küry, S.; Mercier, S.; Moradkhani, K.; Conrad, S.; Besnard, T.; Cogné, B.; Bézieau, S.; Isidor, B.; Adebambo, O.A.; Khan, T.N.; Katsanis, N.; Mollé, A.; Fourgeux, C.; Poschmann, J.; Caro, A.; Rosello, M.; Orellana, C.; Martinez, F.; Niyazov, D.; Lederer, D.; Deprez, M.; Capri, Y.; Kannu, P.; Tabet, A.C.; Levy, J.; Aten, E.; den Hollander, N.; Splitt, M.; Walia, J.; Immken, L.L.; Stankiewicz, P.; Rosenfeld, J.A.; McWalter, K.; Suchy, S.; Louie, R.J.; Bell, S.; Stevenson, R.E.; Rousseau, J.; Campeau, P.M.; Willem, C.; Retiere, C.; Yang, X.-J.; Davis, E.E.
Source
In: American Journal of Human Genetics . (American Journal of Human Genetics, 6 May 2021, 108(5):929-941)
Subject
Language
English
ISSN
15376605
00029297
00029297