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Combined family trio and case-control analysis of the COMT Val158Met polymorphism in European patients with anorexia nervosa

✍ Scribed by Gabrovsek, M. ;Brecelj-Anderluh, M. ;Bellodi, L. ;Cellini, E. ;Di Bella, D. ;Estivill, X. ;Fernandez-Aranda, F. ;Freeman, B. ;Geller, F. ;Gratacos, M. ;Haigh, R. ;Hebebrand, J. ;Hinney, A. ;Holliday, J. ;Hu, X. ;Karwautz, A. ;Nacmias, B. ;Ribases, M. ;Remschmidt, H. ;Komel, R. ;Sorbi, S. ;Tomori, M. ;Treasure, J. ;Wagner, G. ;Zhao, J. ;Collier, D.A.


Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
72 KB
Volume
124B
Category
Article
ISSN
0148-7299

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## Abstract The human small‐conductance Ca^2+^‐activated potassium channel gene __KCNN3__ has been involved in mechanisms underlying neuronal function and plasticity. A multiallelic CAG repeat polymorphism within the __KCNN3__ has been associated with schizophrenia and bipolar disorder. We have pre