| 发明名称 |
SPINOCEREBELLAR ATAXIA TYPE 8 AND METHODS OF DETECTION |
| 摘要 |
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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| 申请公布号 |
US2013230849(A9) |
申请公布日期 |
2013.09.05 |
| 申请号 |
US201213589266 |
申请日期 |
2012.08.20 |
| 申请人 |
RANUM LAURA P. W.;KOOB MICHAEL D.;BENZOW KELLIE A.;MOSELEY-ALLDREDGE MELINDA L.;REGENTS OF THE UNIVERSITY OF MINNESOTA |
发明人 |
RANUM LAURA P. W.;KOOB MICHAEL D.;BENZOW KELLIE A.;MOSELEY-ALLDREDGE MELINDA L. |
| 分类号 |
C12N15/00;C12Q1/68;C07H21/04;C12N15/63;G01N33/50 |
主分类号 |
C12N15/00 |
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