Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Dystonia and PARK2[original query] |
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Low frequency of Parkin, Tyrosine Hydroxylase, and GTP Cyclohydrolase I gene mutations in a Danish population of early-onset Parkinson's Disease. European journal of neurology : the official journal of the European Federation of Neurological Societies 2006 Apr 13 (4): 385-90. Hertz J M, Ostergaard K, Juncker I, Pedersen S, Romstad A, Møller L B, Güttler F, Dupont |
Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia. Brain : a journal of neurology 2009 Jul 132 (Pt 7): 1753-63. Clot Fabienne, Grabli David, Cazeneuve Cécile, Roze Emmanuel, Castelnau Pierre, Chabrol Brigitte, Landrieu Pierre, Nguyen Karine, Ponsot Gérard, Abada Myriem, Doummar Diane, Damier Philippe, Gil Roger, Thobois Stéphane, Ward Alana J, Hutchinson Michael, Toutain Annick, Picard Fabienne, Camuzat Agnès, Fedirko Estelle, Sân Chankannira, Bouteiller Delphine, LeGuern Eric, Durr Alexandra, Vidailhet Marie, Brice Alexis, |
Analysis of PARK2 gene exon rearrangements in Russian patients with sporadic Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 2012 Jan 27 (1): 139-42. Semenova Elena V, Shadrina Maria I, Slominsky Pyotr A, Ivanova-Smolenskaya Irina A, Bagyeva Gulbakhar, Illarioshkin Sergei N, Limborska Svetlana |
Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 2012 Oct 27 (12): 1522-9. Kilarski Laura L, Pearson Justin P, Newsway Victoria, Majounie Elisa, Knipe M Duleeka W, Misbahuddin Anjum, Chinnery Patrick F, Burn David J, Clarke Carl E, Marion Marie-Helene, Lewthwaite Alistair J, Nicholl David J, Wood Nicholas W, Morrison Karen E, Williams-Gray Caroline H, Evans Jonathan R, Sawcer Stephen J, Barker Roger A, Wickremaratchi Mirdhu M, Ben-Shlomo Yoav, Williams Nigel M, Morris Huw |
Han Chinese family with early-onset Parkinson's disease carries novel compound heterozygous mutations in the PARK2 gene. Brain and behavior 2019 8 9 (9): e01372. Huang Ting, Gao Chen-Yu, Wu Liang, Gong Peng-Yu, Wang Ji-Zheng, Tian You-Yong, Zhang Ying-Do |
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- Page last updated:Jun 17, 2024
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