发明名称 |
METHODS FOR DIAGNOSING EPISODIC MOVEMENT DISORDERS AND RELATED CONDITIONS |
摘要 |
The present invention provides compositions and methods for research, diagnostic, drug screening, and therapeutic applications related to paroxysmal dystonic choreoathetosis and related conditions. In particular, the present invention provides mutations in the myofibrillogenesis regulator 1 (MR-1) gene associated with such conditions.
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申请公布号 |
US2010227330(A1) |
申请公布日期 |
2010.09.09 |
申请号 |
US20100729773 |
申请日期 |
2010.03.23 |
申请人 |
THE REGENTS OF THE UNIVERSITY OF MICHIGAN |
发明人 |
FINK JOHN K.;RAINIER SHIRLEY |
分类号 |
C12Q1/68;C07H21/04;C12N5/10;C12N15/63;G01N33/53 |
主分类号 |
C12Q1/68 |
代理机构 |
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代理人 |
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主权项 |
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地址 |
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