Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes

Fragile X syndrome (FXS) is mostly caused by a CGG triplet expansion in the fragile X mental retardation 1 gene (FMR1). Up to 60% of affected males fulfill criteria for autism spectrum disorder (ASD), making FXS the most frequent monogenetic cause of syndromic ASD. It is unknown, however, whether no...

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Detalles Bibliográficos
Autores principales: Stepniak, Beata, Kästner, Anne, Poggi, Giulia, Mitjans, Marina, Begemann, Martin, Hartmann, Annette, Van der Auwera, Sandra, Sananbenesi, Farahnaz, Krueger‐Burg, Dilja, Matuszko, Gabriela, Brosi, Cornelia, Homuth, Georg, Völzke, Henry, Benseler, Fritz, Bagni, Claudia, Fischer, Utz, Dityatev, Alexander, Grabe, Hans‐Jörgen, Rujescu, Dan, Fischer, Andre, Ehrenreich, Hannelore
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4693501/
https://www.ncbi.nlm.nih.gov/pubmed/26612855
http://dx.doi.org/10.15252/emmm.201505696

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4693501/
https://www.ncbi.nlm.nih.gov/pubmed/26612855
http://dx.doi.org/10.15252/emmm.201505696

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