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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...
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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
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 |
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