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pro vyhledávání: '"FXR2 protein, human"'
Autor:
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
Publikováno v:
EMBO molecular medicine
EMBO molecular medicine 7(12), 1565-1579 (2015). doi:10.15252/emmm.201505696
EMBO Molecular Medicine
EMBO molecular medicine 7(12), 1565-1579 (2015). doi:10.15252/emmm.201505696
EMBO Molecular Medicine
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::71b324e438d72265352eec6e811e7c58
https://doi.org/10.15252/emmm.201505696
https://doi.org/10.15252/emmm.201505696
