المؤلفون: Walker RM; Medical Genetics Section, Centre for Molecular Medicine and Institute of Genetics and Molecular Medicine, Molecular Medicine Centre, Western General Hospital, University of Edinburgh, Crewe Road, Edinburgh EH4 2XU, UK. R.M.Walker-2@sms.ed.ac.uk, Christoforou A, Thomson PA, McGhee KA, Maclean A, Mühleisen TW, Strohmaier J, Nieratschker V, Nöthen MM, Rietschel M, Cichon S, Morris SW, Jilani O, Stclair D, Blackwood DH, Muir WJ, Porteous DJ, Evans KL

المصدر: Neuroscience letters [Neurosci Lett] 2010 Jun 30; Vol. 478 (1), pp. 9-13. Date of Electronic Publication: 2010 May 07.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Elsevier Scientific Publishers Ireland Country of Publication: Ireland NLM ID: 7600130 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1872-7972 (Electronic) Linking ISSN: 03043940 NLM ISO Abbreviation: Neurosci Lett Subsets: MEDLINE

مواضيع طبية MeSH: Bipolar Disorder/*genetics , Neuregulin-1/*genetics , Schizophrenia/*genetics, 3' Flanking Region ; 5' Flanking Region ; Case-Control Studies ; Genetic Predisposition to Disease ; Genome-Wide Association Study ; Germany ; Haplotypes ; Humans ; Polymorphism, Single Nucleotide ; Scotland