Gauthier_2011_Hum.Genet_130_563

Reference

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 : Gauthier_2011_Hum.Genet_130_563
ESTHER : Gauthier_2011_Hum.Genet_130_563
PubMedSearch : Gauthier_2011_Hum.Genet_130_563
PubMedID: 21424692

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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 (2011)
Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia
Hum Genet 130 :563

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 (2011)
Hum Genet 130 :563