HEREDITAS ›› 2009, Vol. 31 ›› Issue (6): 605-610.doi: 10.3724/SP.J.1005.2009.00605
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TAN Jian-Qiang1;WANG Ping2;HU Qi-Ping1;LI Song-Feng1;SHU Wei1;MA Jun1;FANG Ling1;HUA Rong1;DING Ye1;YUAN Zhi-Gang1
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Abstract: To characterize the distributions and subtypes of the spinocerebellar ataxias (SCA) in Guangxi region, the SCAl, SCA2, SCA3/MJD, SCA6, SCA7 and SCA12 (CAG)n mutations were analyzed by polymerase chain reaction (PCR) and capillary electrophoresis (CE). The SCA3/MJD mutation was detected in a total of 21 SCA patients and 19 presymptomatic individuals from 6 SCA families and their CAG repeat numbers were 59~70 and 60~73, respectively. No (CAG)n mutations of SCA1, SCA2, SCA6, SCA7 and SCA12 were detected. This study showed that SCA in Guangxi region is mostly SCA3/MJD subtype and the CAG repeats are smaller than those reported in other regions previously.
TAN Jian-Qiang, WANG Ping, HU Qi-Ping, LI Song-Feng, SHU Wei, MA Jun, FANG Ling, HUA Rong, DING Ye, YUAN Zhi-Gang. Gene diagnosis and CAG repeat analysis of spinocerebellar ataxia cases of Guangxi region[J]. HEREDITAS, 2009, 31(6): 605-610.
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URL: http://www.chinagene.cn/EN/10.3724/SP.J.1005.2009.00605
http://www.chinagene.cn/EN/Y2009/V31/I6/605