Mutation detection in long QT syndrome: a comprehensive set of primers and PCR conditions

被引：25

作者：

Syrris, P

Murray, A

Carter, ND

McKenna, WM

Jeffery, S

机构：

[1] St George Hosp, Sch Med, Med Genet Unit, London SW17 0RE, England

[2] St George Hosp, Sch Med, Dept Cardiol Sci, London SW17 0RE, England

来源：

JOURNAL OF MEDICAL GENETICS | 2001年 / 38卷 / 10期

关键词：

D O I：

10.1136/jmg.38.10.705

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：705 / 710

页数：6

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