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US08748096B2 Spinocerebellar ataxia type 8 and methods of detection 有权
8型脊髓小脑共济失调和检测方法

Spinocerebellar ataxia type 8 and methods of detection
Abstract:
The present invention provides an isolated nucleic acid molecule containing a repeat region of an isolated spinocerebellar ataxia type 8 (SCA8) coding sequence, the coding sequence located within the long arm of chromosome 13, and the complement of the nucleic acid molecule. Diagnostic methods based on identification of this repeat region are also provided.
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