发明申请
US20070190555A1 Methods of detecting mutations associated with ataxia-ocular apraxia 2 (AOA2) 有权
检测与共济失调 - 眼睛不适2(AOA2)相关突变的方法

Methods of detecting mutations associated with ataxia-ocular apraxia 2 (AOA2)
摘要:
Methods of identifying polymorphisms associated with ataxia-ocular apraxia 2 (AOA2), are described. The polymorphisms associated with AOA2 include specific mutations in the senataxin (SETX) gene. Also described are methods of diagnosis of AOA2, as well as methods of assessing an individual for carrier status for AOA2.
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