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2011
Mark Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders.
Chaste, Pauline ; Clement, Nathalie ; Botros, Hany Goubran ; Guillaume, Jean-Luc ; Konyukh, Marina ; Pagan, Cécile ; Scheid, Isabelle ; Nygren, Gudrun ; Anckarsäter, Henrik ^LU and Råstam, Maria ^LU , et al. (2011) In Journal of Pineal Research 51(4). p.394-399
- Contribution to journal › Article

your query:: Remove keywords: we found a splice site mutation in ASMT (IVS5+2T>C) and one stop mutation in MTNR1A (Y170X) — detected exclusively in patients with ADHD — for which biochemical analyses indicated that they abolish the activity of ASMT and MTNR1A. These genetic and functional results represent the first comprehensive ascertainment of melatonin signaling deficiency in ADHD.