Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndrome

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作者： Bertelsen,B. ^[1] ; Melchior,L. ^[2] ; Jensen,L.R. ^[3] ; Groth,C. ^[4] ; Glenth?j,B. ^[5] ; Rizzo,R. ^[6] ; Debes,N.M. ^[7] ; Skov,L. ; Br?ndum-Nielsen,K. ; Paschou,P. ; Silahtaroglu,A. ; Tümer,Z.

作者单位： Institute for Cellular and Molecular Medicine, University of CopenhagenCopenhagen, Denmark ^[1] Center for Neuropsychiatric Schizophrenia Research, Center for Clinical Intervention and ^[2] Department of Molecular Biology and Genetics, Democritus University of ThraceAlexandroupoli, Greece ^[3] Section of Child Neuropsychiatry, Department of Pediatrics, University of CataniaCatania, Italy ^[4] Applied Human Molecular Genetics, Kennedy Center, Copenhagen University HospitalGlostrup, Denmark ^[5] Tourette Clinic, Department of Pediatrics, Herlev University HospitalHerlev, Denmark ^[6] Institute for Human Genetics, Ernst-Moritz-Arndt-University GreifswaldGriefswald, Germany ^[7]

关键词 ADHD IMMP2L intronic deletions OCD susceptibility gene Tourette syndrome

发布时间 2020-02-26

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