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A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample.
Buervenich S, Carmine A, Galter D, Shahabi HN, Johnels B, Holmberg B, Ahlberg J, Nissbrandt H, Eerola J, Hellström O, Tienari PJ, Matsuura T, Ashizawa T, Wüllner U, Klockgether T, Zimprich A, Gasser T, Hanson M, Waseem S, Singleton A, McMahon FJ, Anvret M, Sydow O, Olson L. Buervenich S, et al. Among authors: galter d. Arch Neurol. 2005 Jan;62(1):74-8. doi: 10.1001/archneur.62.1.74. Arch Neurol. 2005. PMID: 15642852
Association of a polymorphism in the ABCB1 gene with Parkinson's disease.
Westerlund M, Belin AC, Anvret A, Håkansson A, Nissbrandt H, Lind C, Sydow O, Olson L, Galter D. Westerlund M, et al. Among authors: galter d. Parkinsonism Relat Disord. 2009 Jul;15(6):422-4. doi: 10.1016/j.parkreldis.2008.11.010. Epub 2009 Feb 3. Parkinsonism Relat Disord. 2009. PMID: 19196542
NURR1 promoter polymorphisms: Parkinson's disease, schizophrenia, and personality traits.
Carmine A, Buervenich S, Galter D, Jönsson EG, Sedvall GC, Farde L, Gustavsson JP, Bergman H, Chowdari KV, Nimgaonkar VL, Anvret M, Sydow O, Olson L. Carmine A, et al. Among authors: galter d. Am J Med Genet B Neuropsychiatr Genet. 2003 Jul 1;120B(1):51-7. doi: 10.1002/ajmg.b.20033. Am J Med Genet B Neuropsychiatr Genet. 2003. PMID: 12815740
81 results