| 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 as set forth in one of SEQ ID Numbers: 1-72. |
| 申请公布号 |
US8129142(B2) |
申请公布日期 |
2012.03.06 |
| 申请号 |
US20040567424 |
申请日期 |
2004.08.06 |
| 申请人 |
MULLEY JOHN CHARLES;HARKIN LOUISE ANNE;DIBBENS LEANNE MICHELLE;PHILLIPS HILARY ANNE;HERON SARAH ELIZABETH;BERKOVIC SAMUEL FRANK;SCHEFFER INGRID EILEEN;DAVY ANNE;BIONOMICS LIMITED |
发明人 |
MULLEY JOHN CHARLES;HARKIN LOUISE ANNE;DIBBENS LEANNE MICHELLE;PHILLIPS HILARY ANNE;HERON SARAH ELIZABETH;BERKOVIC SAMUEL FRANK;SCHEFFER INGRID EILEEN;DAVY ANNE |
| 分类号 |
C12N15/12;C07H21/00;C07K14/47;C07K14/705;C12N5/10;C12N15/63;C12Q1/68 |
主分类号 |
C12N15/12 |
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