Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons

Author:

Bell Scott,Rousseau Justine,Peng Huashan,Aouabed Zahia,Priam Pierre,Theroux Jean-Francois,Jefri Malvin,Tanti Arnaud,Wu Hanrong,Kolobova Ilaria,Silviera Heika,Manzano-Vargas Karla,Ehresmann Sophie,Hamdan Fadi F.,Hettige Nuwan,Zhang Xin,Antonyan Lilit,Nassif Christina,Ghaloul-Gonzalez Lina,Sebastian Jessica,Vockley Jerry,Begtrup Amber G.,Wentzensen Ingrid M.,Crunk Amy,Nicholls Robert D.,Herman Kristin C.,Deignan Joshua L.,Al-Hertani Walla,Efthymiou Stephanie,Salpietro Vincenzo,Miyake Noriko,Makita Yoshio,Matsumoto Naomichi,Østern Rune,Houge Gunnar,Hafström Maria,Fassi Emily,Houlden Henry,Klein Wassink-Ruiter Jolien S.,Nelson Dominic,Goldstein Amy,Dabir Tabib,van Gils Julien,Bourgeron Thomas,Delorme Richard,Cooper Gregory M.,Martinez Jose E.,Finnila Candice R.,Carmant Lionel,Lortie Anne,Oegema Renske,van Gassen Koen,Mehta Sarju G.,Huhle Dagmar,Abou Jamra Rami,Martin Sonja,Brunner Han G.,Lindhout Dick,Au Margaret,Graham John M.,Coubes Christine,Turecki Gustavo,Gravel Simon,Mechawar Naguib,Rossignol Elsa,Michaud Jacques L.,Lessard Julie,Ernst Carl,Campeau Philippe M.

Funder

Ministry of Education, Culture, Sports, Science and Technology

Ministry of Health, Labour and Welfare

Canada Research Chairs

Japan Agency for Medical Research and Development

Genome Canada

Consejo Nacional de Ciencia y Tecnología

Génome Québec

Japan Science and Technology Agency

Fonds de Recherche du Québec - Santé

Canadian Institutes of Health Research

Mitacs

Takeda Science Foundation

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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