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Publication date
2016 11
Authors
Caubit, X Gubellini, P Andrieux, J Roubertoux, PL Metwaly, M Jacq, B Fatmi, A Had-Aissouni, L Kwan, KY Salin, P Carlier, M Lieden, A Rudd, E Shinawi, M Vincent-Delorme, C Cuisset, JM Lemaitre, MP Abderrehamane, F Duban, B Lemaitre, JF Woolf, AS Bockenhauer, D Severac, D Dubois, E Zhu, Y Sestan, N Garratt, AN Goff, LKL Fasano, L
Author KI Usernames
Lieden, A|agneli Liedén, A|agneli
Pubmed ID
27668656
Journal
Nature genetics
Doctype
Article
KI Connection
Låg
Mesh SV
Autismspektrumstörning Djur Gendeletion Haploinsufficiens Heterozygot Homeodomänproteiner Kromosomdeletion Kvinnlig Manlig Människa Människokromosomer, par 19 Möss Möss, inavlade CBA Neocortex Nervceller Neurogenes Reglering av genuttryck, utveckling Synapser Transkriptionsfaktorer
Mesh EN
Autism Spectrum Disorder Chromosome Deletion Chromosomes, Human, Pair 19 Gene Deletion Gene Expression Regulation, Developmental Haploinsufficiency Heterozygote Homeodomain Proteins Mice, Inbred CBA Neocortex Neurogenesis Neurons Synapses Transcription Factors
First date
2016-11-20T10:46:36.604Z