Trio study and meta-analysis support the association of genetic variation at the serotonin transporter with early-onset obsessive-compulsive disorder.
第一作者:
Susanne,Walitza
第一单位:
University Clinics for Child and Adolescent Psychiatry, University of Zürich, Switzerland; Department of Child and Adolescent Psychiatry and Psychotherapy, University of Würzburg, Germany; Neuroscience Center Zürich, University of Zürich and ETH Zürich, Switzerland. Electronic address: Susanne.Walitza@kjpdzh.ch.
作者:
医学主题词
成年人(Adult);发病年龄(Age of Onset);儿童(Child);遗传关联研究(Genetic Association Studies);疾病遗传易感性(Genetic Predisposition to Disease);遗传变异(Genetic Variation);人类(Humans);强迫性障碍(Obsessive-Compulsive Disorder);血清素质膜转运蛋白质类(Serotonin Plasma Membrane Transport Proteins)
DOI
10.1016/j.neulet.2014.07.038
PMID
25093702
发布时间
2025-05-29
基金项目
Z01 MH000336/ImNIH/Intramural NIH HHS/United States
ZIA MH000336/ImNIH/Intramural NIH HHS/United States
MH000336-30/MH/NIMH NIH HHS/United States
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Neuroscience letters
100-3页
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