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Title : Novel mutations in NLGN3 causing autism spectrum disorder and cognitive impairment - Quartier_2019_Hum.Mutat_40_2021 |
Author(s) : Quartier A , Courraud J , Thi Ha T , McGillivray G , Isidor B , Rose K , Drouot N , Savidan MA , Feger C , Jagline H , Chelly J , Shaw M , Laumonnier F , Gecz J , Mandel JL , Piton A |
Ref : Hum Mutat , 40 :2021 , 2019 |
Abstract : Quartier_2019_Hum.Mutat_40_2021 |
ESTHER : Quartier_2019_Hum.Mutat_40_2021 |
PubMedSearch : Quartier_2019_Hum.Mutat_40_2021 |
PubMedID: 31184401 |
Gene_locus related to this paper: human-NLGN3 |
Title : Autism and nonsyndromic mental retardation associated with a de novo mutation in the NLGN4X gene promoter causing an increased expression level - Daoud_2009_Biol.Psychiatry_66_906 |
Author(s) : Daoud H , Bonnet-Brilhault F , Vedrine S , Demattei MV , Vourc'h P , Bayou N , Andres CR , Barthelemy C , Laumonnier F , Briault S |
Ref : Biological Psychiatry , 66 :906 , 2009 |
Abstract : Daoud_2009_Biol.Psychiatry_66_906 |
ESTHER : Daoud_2009_Biol.Psychiatry_66_906 |
PubMedSearch : Daoud_2009_Biol.Psychiatry_66_906 |
PubMedID: 19545860 |
Title : X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family - Laumonnier_2004_Am.J.Hum.Genet_74_552 |
Author(s) : Laumonnier F , Bonnet-Brilhault F , Gomot M , Blanc R , David A , Moizard MP , Raynaud M , Ronce N , Lemonnier E , Calvas P , Laudier B , Chelly J , Fryns JP , Ropers HH , Hamel BC , Andres C , Barthelemy C , Moraine C , Briault S |
Ref : American Journal of Human Genetics , 74 :552 , 2004 |
Abstract : Laumonnier_2004_Am.J.Hum.Genet_74_552 |
ESTHER : Laumonnier_2004_Am.J.Hum.Genet_74_552 |
PubMedSearch : Laumonnier_2004_Am.J.Hum.Genet_74_552 |
PubMedID: 14963808 |
Gene_locus related to this paper: human-NLGN4X |