MUTATIONS IN AND GENOMIC STRUCTURE OF HERG - A LONG QT SYNDROME GENE

• 收藏
• 分享

专利权人:

UNIVERSITY OF UTAH RESEARCH FOUNDATION

发明人:

KEATING, MARK, T.,SPLAWSKI, IGOR

申请号：

WO1999US16337

公开号：

WO0006772(A1)

申请日:

1999.07.20

申请国别(地区):

世界知识产权组织国际局

年份:

2000

代理人:

摘要：

The invention relates to the determination of the genomic structure of HERG which is a gene associated with long QT syndrome. The sequences of the 15 intron/exon junctions has been determined and this information is useful in devising primers for amplifying and sequencing across all of the exons of the gene. This is useful for determining the presence or absence of mutations which are known to cause long QT syndrome. Also disclosed are many new mutations in HERG which have been found to be associated with long QT syndrome.

来源网站：

中国工程科技知识中心

来源网址：

http://www.ckcest.cn/home/