학술논문
Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons
Document Type
Article
Author
Bell, S.; Peng, H.; Aouabed, Z.; Theroux, J.-F.; Jefri, M.; Tanti, A.; Wu, H.; Kolobova, I.; Silviera, H.; Manzano-Vargas, K.; Hettige, N.; Zhang, X.; Antonyan, L.; Turecki, G.; Mechawar, N.; Ernst, C.; Rousseau, J.; Ehresmann, S.; Hamdan, F.F.; Nassif, C.; Rossignol, E.; Michaud, J.L.; Campeau, P.M.; Priam, P.; Lessard, J.; Ghaloul-Gonzalez, L.; Sebastian, J.; Vockley, J.; Nicholls, R.D.; Begtrup, A.G.; Wentzensen, I.M.; Crunk, A.; Herman, K.C.; Deignan, J.L.; Al-Hertani, W.; Efthymiou, S.; Salpietro, V.; Houlden, H.; Miyake, N.; Matsumoto, N.; Makita, Y.; Østern, R.; Hafström, M.; Houge, G.; Fassi, E.; Klein Wassink-Ruiter, J.S.; Gravel, S.; Nelson, D.; Goldstein, A.; Dabir, T.; van Gils, J.; Bourgeron, T.; Delorme, R.; Cooper, G.M.; Finnila, C.R.; Martinez, J.E.; Carmant, L.; Lortie, A.; Oegema, R.; van Gassen, K.; Mehta, S.G.; Huhle, D.; Abou Jamra, R.; Martin, S.; Brunner, H.G.; Lindhout, D.; Au, M.; Graham, J.M.; Coubes, C.
Source
In: American Journal of Human Genetics . (American Journal of Human Genetics, 2 May 2019, 104(5):815-834)
Subject
Language
English
ISSN
15376605
00029297
00029297