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Mottron L

References (2)

Title : Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia - Gauthier_2011_Hum.Genet_130_563
Author(s) : Gauthier J , Siddiqui TJ , Huashan P , Yokomaku D , Hamdan FF , Champagne N , Lapointe M , Spiegelman D , Noreau A , Lafreniere RG , Fathalli F , Joober R , Krebs MO , DeLisi LE , Mottron L , Fombonne E , Michaud JL , Drapeau P , Carbonetto S , Craig AM , Rouleau GA
Ref : Hum Genet , 130 :563 , 2011
Abstract :
PubMedSearch : Gauthier_2011_Hum.Genet_130_563
PubMedID: 21424692

Title : NLGN3\/NLGN4 gene mutations are not responsible for autism in the Quebec population - Gauthier_2005_Am.J.Med.Genet.B.Neuropsychiatr.Genet_132B_74
Author(s) : Gauthier J , Bonnel A , St-Onge J , Karemera L , Laurent S , Mottron L , Fombonne E , Joober R , Rouleau GA
Ref : American Journal of Medicine Genet B Neuropsychiatr Genet , 132B :74 , 2005
Abstract :
PubMedSearch : Gauthier_2005_Am.J.Med.Genet.B.Neuropsychiatr.Genet_132B_74
PubMedID: 15389766
Gene_locus related to this paper: human-NLGN4X