SPTBN2 GENE ASSOCIATED WITH SPINOCEREBELLAR ATAXIA TYPE 5 AND METHODS OF USE
摘要
The present invention provides methods that include analyzing an SPTBN2 polynucleotide, and determining whether the SPTBN2 polynucleotide includes a mutation. The methods may be used to identify a subject that is at risk or not at risk for developing spinocerebellar ataxia type 5. The present invention also provides isolated polynucleotides having a mutation present in an SPTBN2 polynucleotide.
申请公布号
CA2598281(C)
申请公布日期
2016.08.09
申请号
CA20062598281
申请日期
2006.02.22
申请人
REGENTS OF THE UNIVERSITY OF MINNESOTA
发明人
RANUM, LAURA P. W.;IKEDA, YOSHIO;DICK, KATHERINE A.;DAY, JOHN W.;SCHUT, LAWRENCE J.