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Novel mutations in the CYP7B1 gene cause hereditary spastic paraplegia.
Mov Disord. 2011 Jun;26(7):1354-6. doi: 10.1002/mds.23466. Epub 2011 Mar 30.
Mov Disord. 2011.
PMID: 21452256
No abstract available.
Association study of clusterin polymorphism rs11136000 with late onset Alzheimer's disease in Chinese Han population.
Ma JF, Liu LH, Zhang Y, Wang Y, Deng YL, Huang Y, Wang G, Xu W, Cui PJ, Fei QZ, Ding JQ, Tang HD, Chen SD.
Ma JF, et al. Among authors: fei qz.
Am J Alzheimers Dis Other Demen. 2011 Dec;26(8):627-30. doi: 10.1177/1533317511432735. Epub 2012 Jan 31.
Am J Alzheimers Dis Other Demen. 2011.
PMID: 22296908
Free PMC article.
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Lack of association between ATP13A2 Ala746Thr variant and Parkinson's disease in Han population of mainland China.
Fei QZ, Cao L, Xiao Q, Zhang T, Zheng L, Wang XJ, Wang G, Zhou HY, Wang Y, Chen SD.
Fei QZ, et al.
Neurosci Lett. 2010 May 14;475(2):61-3. doi: 10.1016/j.neulet.2010.03.018. Epub 2010 Mar 19.
Neurosci Lett. 2010.
PMID: 20227461
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The association between two single nucleotide polymorphisms within the insulin-degrading enzyme gene and Alzheimer's disease in a Chinese Han population.
Cui PJ, Cao L, Wang Y, Deng YL, Xu W, Wang G, Zhang Y, Zheng L, Fei QZ, Zhang T, Chen SD.
Cui PJ, et al. Among authors: fei qz.
J Clin Neurosci. 2012 May;19(5):745-9. doi: 10.1016/j.jocn.2011.08.036.
J Clin Neurosci. 2012.
PMID: 22502914
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