发明名称 |
MUTATIONS IN ION CHANNELS |
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 |
CA2454073(A1) |
申请公布日期 |
2003.01.30 |
申请号 |
CA20022454073 |
申请日期 |
2002.07.08 |
申请人 |
BIONOMICS LIMITED |
发明人 |
HARKIN, LOUISE ANNE;MULLEY, JOHN CHARLES;DIBBENS, LEANNE MICHELLE;SCHEFFER, INGRID EILEEN;HERON, SARAH ELIZABETH;PHILLIPS, HILARY ANNE;BERKOVIC, SAMUEL FRANK |
分类号 |
A01K67/02;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;C12N15/09;C12P21/02;C12P21/08;C12Q1/02;C12Q1/68;G01N33/15;G01N33/50;G01N33/68;(IPC1-7):C12N15/09 |
主分类号 |
A01K67/02 |
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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