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The D216H variant in the DYT1 gene: a susceptibility factor for dystonia in familial cases?
Brüggemann, N; Kock, N; Lohmann, K; König, I R; Rakovic, A; Hagenah, J; Schmidt, A; Ziegler, A; Jabusch, H C; Siebner, H; Altenmüller, E; Münchau, A; Klein, C.
Affiliation
  • Brüggemann N; Department of Neurology, University of Lübeck, Germany.
Neurology ; 72(16): 1441-3, 2009 Apr 21.
Article in En | MEDLINE | ID: mdl-19380705

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polymorphism, Genetic / Molecular Chaperones / Genetic Predisposition to Disease / Dystonia Type of study: Prognostic_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Neurology Year: 2009 Document type: Article Affiliation country: Germany Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polymorphism, Genetic / Molecular Chaperones / Genetic Predisposition to Disease / Dystonia Type of study: Prognostic_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Neurology Year: 2009 Document type: Article Affiliation country: Germany Country of publication: United States