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Heterozygous carriers of a Parkin or PINK1 mutation share a common functional endophenotype.
van Nuenen, B F L; Weiss, M M; Bloem, B R; Reetz, K; van Eimeren, T; Lohmann, K; Hagenah, J; Pramstaller, P P; Binkofski, F; Klein, C; Siebner, H R.
Affiliation
  • van Nuenen BF; Department of Neurology, Christian-Albrechts University, Kiel, Germany.
Neurology ; 72(12): 1041-7, 2009 Mar 24.
Article in En | MEDLINE | ID: mdl-19038850
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Protein Kinases / Genetic Predisposition to Disease / Parkinsonian Disorders / Ubiquitin-Protein Ligases / Frontal Lobe / Neuronal Plasticity Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Neurology Year: 2009 Document type: Article Affiliation country: Germany Country of publication: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Protein Kinases / Genetic Predisposition to Disease / Parkinsonian Disorders / Ubiquitin-Protein Ligases / Frontal Lobe / Neuronal Plasticity Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Neurology Year: 2009 Document type: Article Affiliation country: Germany Country of publication: United States