Zinc deficiency and low enterocyte zinc transporter expression in human patients with autism related mutations in SHANK3.
authors
Contributors
Institute for Anatomy and Cell Biology ; Universität Ulm - Ulm University [Ulm, Allemagne],
WG Molecular Analysis of Synaptopathies ; Universität Ulm - Ulm University [Ulm, Allemagne],
Eberhard Karls University Tübingen,
Génétique humaine et fonctions cognitives - Human Genetics and Cognitive Functions (GHFC (UMR_3571 / U-Pasteur_1)) ; Institut Pasteur [Paris]-Université Paris Diderot - Paris 7 (UPD7)-Centre National de la Recherche Scientifique (CNRS),
TMB has received support from the Innovative Medicines Initiative Joint Undertaking under grant agreement n° 115300, resources of which are composed of financial contribution from the European Union’s Seventh Framework Programme (FP7/2007–2013) and EFPIA companies’ in kind contribution. Furthermore by the Helmholtz Gesellschaft (“RNA Dysmetabolism in ALS and FTD” to TMB) and the Deutsche Forschungsgemeinschaft (DFG SBF1149 to TMB). AMG was supported by the Else-Kröner-Fresenius Stiftung (214_A251). The authors would like to acknowledge networking support by the COST Action TD13.,
European Project: 115300,EC:FP7:SP1-JTI,IMI-JU-03-2010,EU-AIMS(2012)
Publication Date: 2017-03-27
Last GoTriple update: 2022-08-23
Publisher
HAL CCSD,
Nature Publishing Group
Provider: Isidore
Producer: Hyper Article en Ligne - Sciences de l'Homme et de la Société
License: Creative Commons, Other
Conditions of Access: Other, Open Access
Disciplines