Detection of large deletion mutations in the SERPINC1 gene causing hereditary antithrombin deficiency by multiplex ligation-dependent probe amplification (MLPA)

被引：18
|
作者：
Lee, S. -T. [1 ]
Kim, H. -J. [1 ]
Kim, D. -K. [2 ]
Schuit, R. J. L. [3 ]
Kim, S. -H. [1 ]
机构：
[1] Sungkyunkwan Univ, Sch Med, Dept Lab Med & Genet, Samsung Med Ctr, Seoul 135710, South Korea
[2] Sungkyunkwan Univ, Sch Med, Dept Internal Med, Samsung Med Ctr, Seoul, South Korea
[3] MRC Holland, Amsterdam, Netherlands
来源：
JOURNAL OF THROMBOSIS AND HAEMOSTASIS | 2008年 / 6卷 / 04期
关键词：
D O I：
10.1111/j.1538-7836.2008.02905.x
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：701 / 703
页数：3
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