| Title : Synapse and primary cilia dysfunctions in Autism Spectrum Disorders. Avenues to normalize these functions - Hauw_2024_Rev.Neurol.(Paris)__ |
| Author(s) : Hauw JJ , Hausser-Hauw C , Barthelemy C |
| Ref : Rev Neurol (Paris) , : , 2024 |
| Abstract : |
| PubMedSearch : Hauw_2024_Rev.Neurol.(Paris)__ |
| PubMedID: 38925998 |
| 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 : |
| 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 : |
| PubMedSearch : Laumonnier_2004_Am.J.Hum.Genet_74_552 |
| PubMedID: 14963808 |
| Gene_locus related to this paper: human-NLGN4X |