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1 Ergebnisse
1
Mutations in ACTL6B Cause Neurodevelopmental Deficits and E..:
Bell, Scott
;
Rousseau, Justine
;
Peng, Huashan
...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2019.03.022. , 2019
Link:
https://pasteur.hal.science/pasteur-03325419
RT Journal T1
Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons
UL https://suche.suub.uni-bremen.de/peid=base-ftunivparis:oai:HAL:pasteur-03325419v1&Exemplar=1&LAN=DE A1 Bell, Scott A1 Rousseau, Justine A1 Peng, Huashan A1 Aouabed, Zahia A1 Priam, Pierre A1 Theroux, Jean-Francois A1 Jefri, Malvin A1 Tanti, Arnaud A1 Wu, Hanrong A1 Kolobova, Ilaria A1 Silviera, Heika A1 Manzano-Vargas, Karla A1 Ehresmann, Sophie A1 Hamdan, Fadi, F A1 Hettige, Nuwan A1 Zhang, Xin A1 Antonyan, Lilit A1 Nassif, Christina A1 Ghaloul-Gonzalez, Lina A1 Sebastian, Jessica A1 Vockley, Jerry A1 Begtrup, Amber, G A1 Wentzensen, Ingrid, M A1 Crunk, Amy A1 Nicholls, Robert, D A1 Herman, Kristin, C A1 Deignan, Joshua, L A1 Al-Hertani, Walla A1 Efthymiou, Stephanie A1 Salpietro, Vincenzo A1 Miyake, Noriko A1 Makita, Yoshio A1 Matsumoto, Naomichi A1 Østern, Rune A1 Houge, Gunnar A1 Hafström, Maria A1 Fassi, Emily A1 Houlden, Henry A1 Klein Wassink-Ruiter, Jolien, S A1 Nelson, Dominic A1 Goldstein, Amy A1 Dabir, Tabib A1 van Gils, Julien A1 Bourgeron, Thomas A1 Delorme, Richard A1 Cooper, Gregory, M A1 Martinez, Jose, E A1 Finnila, Candice, R A1 Carmant, Lionel A1 Lortie, Anne A1 Oegema, Renske A1 van Gassen, Koen A1 Mehta, Sarju, G A1 Huhle, Dagmar A1 Abou Jamra, Rami A1 Martin, Sonja A1 Brunner, Han, G A1 Lindhout, Dick A1 Au, Margaret A1 Graham Jr., John, M A1 Coubes, Christine A1 Turecki, Gustavo A1 Gravel, Simon A1 Mechawar, Naguib A1 Rossignol, Elsa A1 Michaud, Jacques, L A1 Lessard, Julie A1 Ernst, Carl A1 Campeau, Philippe, M PB HAL CCSD; Elsevier (Cell Press) YR 2019 K1 ACTL6B K1 genetic engineering K1 intellectual disability K1 neurodevelopment K1 seizure K1 stem cells K1 MESH: Actins K1 MESH: Adult K1 MESH: Child K1 Preschool K1 MESH: Chromatin K1 MESH: Chromosomal Proteins K1 Non-Histone K1 MESH: DNA-Binding Proteins K1 MESH: Dendrites K1 MESH: Epilepsy K1 MESH: Female K1 MESH: Humans K1 MESH: Induced Pluripotent Stem Cells K1 MESH: Infant K1 MESH: Male K1 MESH: Mutation K1 MESH: Neurodevelopmental Disorders K1 MESH: Neurons K1 MESH: Young Adult K1 [SCCO.NEUR]Cognitive science/Neuroscience JF info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2019.03.022 LK http://dx.doi.org/https://pasteur.hal.science/pasteur-03325419 DO https://pasteur.hal.science/pasteur-03325419 SF ELIB - SuUB Bremen
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