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https://doi.org/10.1212/01.WNL.0000130199.57181.7B
| Title: | Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort | Authors: | Tan E.K. Zhao Y. Puong K.Y. Law H.Y. Chan L.L. Yew K. Tan C. Shen H. Chandran V.R. Teoh M.L. Yih Y. Pavanni R. Wong M.C. Ng I.S. |
Issue Date: | 2004 | Publisher: | Lippincott Williams and Wilkins | Citation: | Tan E.K., Zhao Y., Puong K.Y., Law H.Y., Chan L.L., Yew K., Tan C., Shen H., Chandran V.R., Teoh M.L., Yih Y., Pavanni R., Wong M.C., Ng I.S. (2004). Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort. Neurology 63 (2) : 362-363. ScholarBank@NUS Repository. https://doi.org/10.1212/01.WNL.0000130199.57181.7B | Abstract: | Among 367 subjects, the authors analyzed 167 patients with essential tremor, sporadic progressive cerebellar ataxia, multiple-system atrophy, and atypical parkinsonism and 200 healthy control subjects for FMR1 premutation alleles. None of the subjects carried alleles within the premutation range. These findings suggest that in the absence of other supportive clinical or imaging features, the cost-effectiveness of routine fragile X tremor/ataxia syndrome screening in this Asian cohort with movement disorders was low. | Source Title: | Neurology | URI: | http://scholarbank.nus.edu.sg/handle/10635/150237 | ISSN: | 00283878 | DOI: | 10.1212/01.WNL.0000130199.57181.7B |
| Appears in Collections: | Staff Publications |
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