Lack of association between a functional polymorphism of the cytochrome P450 1A2 (CYP1A2) gene and tardive dyskinesia in schizophrenia.

Schulze, T G; Schumacher, J; Müller, D J; Krauss, H; Alfter, D; Maroldt, A; Ahle, G; Maroldt, A O; Novo y Fernández, A; Weber, T; Held, T; Propping, P; Maier, W; Nöthen, M M; Rietschel, M

Schulze, T G; Schumacher, J; Müller, D J; Krauss, H; Alfter, D; Maroldt, A; Ahle, G; Maroldt, A O; Novo y Fernández, A; Weber, T; Held, T; Propping, P; Maier, W; Nöthen, M M; Rietschel, M.

Affiliation

Schulze TG; Department of Psychiatry, University of Bonn, Bonn, Germany. schulze@uchicago.edu

Am J Med Genet ; 105(6): 498-501, 2001 Aug 08.

Article de En | MEDLINE | ID: mdl-11496364

Sujet(s)

Recherche sur Google

Ajouter à My VHL

Imprimer

XML

PubMed Links

Collection: 01-internacional Base de données: MEDLINE Sujet principal: Schizophrénie / Cytochrome P-450 CYP1A2 / Dyskinésie due aux médicaments Type d'étude: Risk_factors_studies Limites: Adult / Female / Humans / Male / Middle aged Langue: En Journal: Am J Med Genet Année: 2001 Type de document: Article Pays d'affiliation: Allemagne Pays de publication: États-Unis d'Amérique

Recherche sur Google

Ajouter à My VHL

Imprimer

XML

PubMed Links