SCA8 repeat expansion: large CTA/CTG repeat alleles in neurological disorders and functional implications-Reference-Cited by-同舟云学术

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SCA8 repeat expansion: large CTA/CTG repeat alleles in neurological disorders and functional implications

Published:2009-02-20 Issue:4 Volume:125 Page:437-444
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

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-Mei

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-009-0641-x.pdf

Reference30 articles.

1. Akira S, Isshiki H, Sugita T, Tanabe O, Kinoshita S, Nishio Y, Nakajima T, Hirano T, Kishimoto T (1990) A nuclear factor for IL-6 expression (NF-IL6) is a member of a C/EBP family. EMBO J 9:1897–1906

2. Baba Y, Uitti RJ, Farrer MJ, Wszolek ZK (2005) Sporadic SCA8 mutation resembling corticobasal degeneration. Parkinsonism Relat Disord 11:147–150

3. Boeve BF (2007) Parkinson-related dementias. Neurol Clin 25:761–781, vii

4. Chen KY, Pan H, Lin MJ, Li YY, Wang LC, Wu YC, Hsiao KM (2007) Length-dependent toxicity of untranslated CUG repeats on Caenorhabditis elegans. Biochem Biophys Res Commun 352:774–779

5. Day JW, Schut LJ, Moseley ML, Durand AC, Ranum LP (2000) Spinocerebellar ataxia type 8: clinical features in a large family. Neurology 55:649–657

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3. Genetic and clinical analyses of spinocerebellar ataxia type 8 in mainland China;Journal of Neurology;2019-08-30

4. PSP-Phenotype in SCA8: Case Report and Systemic Review;The Cerebellum;2018-06-19

5. Parkinsonism in Spinocerebellar Ataxia;BioMed Research International;2015

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