Rare coding variants of the adenosine A3 receptor are increased in autism: on the trail of the serotonin transporter regulome

BACKGROUND: Rare genetic variation is an important class of autism spectrum disorder (ASD) risk factors and can implicate biological networks for investigation. Altered serotonin (5-HT) signaling has been implicated in ASD, and we and others have discovered multiple, rare, ASD-associated variants in...

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Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: Campbell, Nicholas G, Zhu, Chong-Bin, Lindler, Kathryn M, Yaspan, Brian L, Kistner-Griffin, Emily, Hewlett, William A, Tate, Christopher G, Blakely, Randy D, Sutcliffe, James S
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: BioMed Central 2013
Θέματα:
Research
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3882891/
https://ncbi.nlm.nih.gov/pubmed/23953133
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2040-2392-4-28
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