| 发明名称 |
MUTATIONEN IN IONENKANÄLEN |
| 摘要 |
A method of identifying a subject predisposed to a disorder associated with ion channel dysfunction, comprising ascertaining whether at least one of the genes encoding ion channel subunits in said subject has undergone a mutation event such that a cDNA derived from said subject has the sequence set forth in one of SEQ ID NOS: 1-134. |
| 申请公布号 |
AT373089(T) |
申请公布日期 |
2007.09.15 |
| 申请号 |
AT20020748429T |
申请日期 |
2002.07.08 |
| 申请人 |
BIONOMICS LIMITED |
发明人 |
MULLEY, JOHN;HARKIN, LOUISE;DIBBENS, LEANNE;PHILLIPS, HILARY;HERON, SARAH;BERKOVIC, SAMUEL;SCHEFFER, INGRID;WALLACE, ROBYN |
| 分类号 |
A01K67/02;C12N15/09;A01K67/027;A61K31/711;A61K38/00;A61K39/395;A61K45/00;A61K48/00;A61P3/10;A61P3/12;A61P9/06;A61P21/02;A61P21/04;A61P25/02;A61P25/06;A61P25/08;A61P25/14;A61P25/16;A61P25/18;A61P25/22;A61P25/24;A61P25/28;A61P29/02;A61P43/00;C07K14/47;C07K14/705;C07K16/28;C12N1/15;C12N1/19;C12N1/21;C12N5/10;C12P21/02;C12P21/08;C12Q1/02;C12Q1/68;G01N33/15;G01N33/50;G01N33/68 |
主分类号 |
A01K67/02 |
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