https://scholars.lib.ntu.edu.tw/handle/123456789/520048
Title: | COQ2 gene variants associate with cerebellar subtype of multiple system atrophy in Chinese | Authors: | CHIN-HSIEN LIN Tan E.-K. Yang C.-C. Yi Z. RUEY-MEEI WU |
Issue Date: | 2015 | Publisher: | John Wiley and Sons Inc. | Journal Volume: | 30 | Journal Issue: | 3 | Start page/Pages: | 436-437 | Source: | Movement Disorders | URI: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84924545322&doi=10.1002%2fmds.26138&partnerID=40&md5=ed53d58943c486d4cde732a05a63fa3c https://scholars.lib.ntu.edu.tw/handle/123456789/520048 |
ISSN: | 0885-3185 | DOI: | 10.1002/mds.26138 | SDG/Keyword: | cerebellum disease; Chinese; controlled study; coq2 gene; gene; gene frequency; genetic association; genetic code; genetic susceptibility; genetic variability; heterozygote; human; Letter; major clinical study; Parkinson disease; phenotype; priority journal; rare disease; Shy Drager syndrome; Asian continental ancestry group; cerebellum; female; genetics; genotype; male; odds ratio; pathology; Shy Drager syndrome; single nucleotide polymorphism; 4-hydroxybenzoate polyprenyltransferase; transferase; Alkyl and Aryl Transferases; Asian Continental Ancestry Group; Cerebellum; Female; Gene Frequency; Genotype; Humans; Male; Multiple System Atrophy; Odds Ratio; Polymorphism, Single Nucleotide |
Appears in Collections: | 醫學系 |
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