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pro vyhledávání: '"Fatimetou Abderrehamane"'
Autor:
Ahmed Fatmi, Pierre L. Roubertoux, Joris Andrieux, Catherine Vincent-Delorme, Michèle Carlier, Paolo Gubellini, Laurence Had-Aissouni, Fatimetou Abderrehamane, Bénédicte Duban, Agne Liedén, Detlef Bockenhauer, Emeric Dubois, Mehdi Metwaly, Adrian S. Woolf, Nenad Sestan, Dany Severac, Jean Marie Cuisset, Laurent Fasano, Jean François Lemaitre, Marwan Shinawi, Marie Pierre Lemaitre, Lydia Kerkerian-Le Goff, Eva Rudd, Xavier Caubit, Pascal Salin, Bernard Jacq, Alistair N. Garratt, Kenneth Y. Kwan, Ying Zhu
Publikováno v:
Nature Genetics
Nature Genetics, Nature Publishing Group, 2016, 48 (11), pp.1359-1369. ⟨10.1038/ng.3681⟩
Nature Genetics, 2016, 48 (11), pp.1359-1369. ⟨10.1038/ng.3681⟩
Nature genetics
Caubit, X, Gubellini, P, Andrieux, J, Roubertoux, P L, Metwaly, M, Jacq, B, Fatmi, A, Had-Aissouni, L, Kwan, K Y, Salin, P, Carlier, M, Liedén, A, Rudd, E, Shinawi, M, Vincent-Delorme, C, Cuisset, J-M, Lemaitre, M-P, Fatimetou, A, Duban, B, Lemaitre, J-F, Woolf, A S, Bockenhauer, D, Severac, D, Dubois, E, Zhu, Y, Sestan, N, Garratt, A N, Kerkerian-Le Goff, L & Fasano, L 2016, ' TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons ', Nature Genetics, vol. 48, pp. 1359-1369 . https://doi.org/10.1038/ng.3681
Nature Genetics, Nature Publishing Group, 2016, 48 (11), pp.1359-1369. ⟨10.1038/ng.3681⟩
Nature Genetics, 2016, 48 (11), pp.1359-1369. ⟨10.1038/ng.3681⟩
Nature genetics
Caubit, X, Gubellini, P, Andrieux, J, Roubertoux, P L, Metwaly, M, Jacq, B, Fatmi, A, Had-Aissouni, L, Kwan, K Y, Salin, P, Carlier, M, Liedén, A, Rudd, E, Shinawi, M, Vincent-Delorme, C, Cuisset, J-M, Lemaitre, M-P, Fatimetou, A, Duban, B, Lemaitre, J-F, Woolf, A S, Bockenhauer, D, Severac, D, Dubois, E, Zhu, Y, Sestan, N, Garratt, A N, Kerkerian-Le Goff, L & Fasano, L 2016, ' TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons ', Nature Genetics, vol. 48, pp. 1359-1369 . https://doi.org/10.1038/ng.3681
International audience; TSHZ3, which encodes a zinc-finger transcription factor, was recently positioned as a hub gene in a module of the genes with the highest expression in the developing human neocortex, but its functions remained unknown. Here we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1526d52f0caf1ad65c8793faee92cf7
https://hal.archives-ouvertes.fr/hal-01432295
https://hal.archives-ouvertes.fr/hal-01432295