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Mutations in ACTL6B Cause Neurodevelopmental Deficits and E..:

Bell, S ; Rousseau, J ; Peng, H...
https://discovery.ucl.ac.uk/id/eprint/10078636/1/AJHG%20manuscript%20ACTL6B.pdf. , 2019

Link: https://discovery.ucl.ac.uk/id/eprint/10078636/1/AJHG%..

RT Journal
T1 <Title>Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftucl:oai:eprints.ucl.ac.uk.OAI2:10078636&Exemplar=1&LAN=DE
				
A1 Bell, S
A1 Rousseau, J
A1 Peng, H
A1 Aouabed, Z
A1 Priam, P
A1 Theroux, J-F
A1 Jefri, M
A1 Tanti, A
A1 Wu, H
A1 Kolobova, I
A1 Silviera, H
A1 Manzano-Vargas, K
A1 Ehresmann, S
A1 Hamdan, FF
A1 Hettige, N
A1 Zhang, X
A1 Antonyan, L
A1 Nassif, C
A1 Ghaloul-Gonzalez, L
A1 Sebastian, J
A1 Vockley, J
A1 Begtrup, AG
A1 Wentzensen, IM
A1 Crunk, A
A1 Nicholls, RD
A1 Herman, KC
A1 Deignan, JL
A1 Al-Hertani, W
A1 Efthymiou, S
A1 Salpietro, V
A1 Miyake, N
A1 Makita, Y
A1 Matsumoto, N
A1 Ostern, R
A1 Houge, G
A1 Hafstrom, M
A1 Fassi, E
A1 Houlden, H
A1 Wassink-Ruiter, JSK
A1 Nelson, D
A1 Goldstein, A
A1 Dabir, T
A1 van Gils, J
A1 Bourgeron, T
A1 Delorme, R
A1 Cooper, GM
A1 Martinez, JE
A1 Finnila, CR
A1 Carmant, L
A1 Lortie, A
A1 Oegema, R
A1 van Gassen, K
A1 Mehta, SG
A1 Huhle, D
A1 Abou Jamra, R
A1 Martin, S
A1 Brunner, HG
A1 Lindhout, D
A1 Au, M
A1 Graham, JM
A1 Coubes, C
A1 Turecki, G
A1 Gravel, S
A1 Mechawar, N
A1 Rossignol, E
A1 Michaud, JL
A1 Lessard, J
A1 Ernst, C
A1 Campeau, PM
PB CELL PRESS
YR 2019
K1 intellectual disability
K1 seizure
K1 ACTL6B
K1 stem cells
K1 genetic engineering
K1 neurodevelopment
JF https://discovery.ucl.ac.uk/id/eprint/10078636/1/AJHG%20manuscript%20ACTL6B.pdf
LK http://dx.doi.org/https://discovery.ucl.ac.uk/id/eprint/10078636/1/AJHG%20manuscript%20ACTL6B.pdf
DO https://discovery.ucl.ac.uk/id/eprint/10078636/1/AJHG%20manuscript%20ACTL6B.pdf
SF ELIB - SuUB Bremen

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