Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Ataxia and ATXN8[original query] |
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SCA8 repeat expansion: large CTA/CTG repeat alleles in neurological disorders and functional implications. Human genetics 2009 May 125 (4): 437-44. Wu Yih-Ru, Chen I-Cheng, Soong Bing-Wen, Kao Shih-Huan, Lee Ghin-Chueh, Huang Shu-Yi, Fung Hon-Chung, Lee-Chen Guey-Jen, Chen Chiung-M |
ATXN8 -62 G/A promoter polymorphism and risk of Taiwanese Parkinson's disease. European journal of neurology : the official journal of the European Federation of Neurological Societies 2012 Nov 19 (11): 1462-9. Chen I-C, Wu Y-R, Yang S-J, Kao S-H, Chen Y-C, Chang K-H, Lee C-M, Lee-Chen G-J, Chen C |
Spinocerebellar ataxias in Venezuela: genetic epidemiology and their most likely ethnic descent. Journal of human genetics 2015 Nov . Paradisi Irene, Ikonomu Vassiliki, Arias Serg |
Molecular epidemiology of hereditary ataxia in Finland. BMC neurology 2021 10 21 (1): 382. Lipponen Joonas, Helisalmi Seppo, Raivo Joose, Siitonen Ari, Doi Hiroshi, Rusanen Harri, Lehtilahti Maria, Ryytty Mervi, Laakso Markku, Tanaka Fumiaki, Majamaa Kari, Kytövuori Lau |
STUB1 Mutations as Possible Genetic Modifiers in Spinocerebellar Ataxia Type 8. Movement disorders : official journal of the Movement Disorder Society 2024 7 . Raquel Baviera-Muñoz, Lidón Carretero-Vilarroig, Ana Pedro-Ibor, Teresa Jaijo, Andrea Del Valle-Carranza, Irene Martínez-Torres, Jose M Millán, Luis Bataller, Elena All |
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