| 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 |
| Gene_locus related to this paper: human-NLGN3 |
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 (2019)
Novel mutations in NLGN3 causing autism spectrum disorder and cognitive impairment
Hum Mutat
40 :2021
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 (2019)
Hum Mutat
40 :2021