Genotyping method for point mutation detection in the endothelial nitric oxide synthase exon 7 using fluorescent probes. Clinical validation in systemic sclerosis patients

被引:11
作者
Biondi, ML
Marasini, B
Leviti, S
Turri, O
Bernini, M
Seminati, R
Porreca, W
Guagnellini, E
机构
[1] Azienda Osped San Paolo, Lab Chim Clin & Microbiol, I-20142 Milan, Italy
[2] Univ Milan, Dept Med Surg & Dent, S Paolo Hosp, Milan, Italy
关键词
fluorescent probes; NO-synthase exon 7 polymorphism; systemic sclerosis;
D O I
10.1515/CCLM.2001.043
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
引用
收藏
页码:281 / 282
页数:2
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