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

来源：

CLINICAL CHEMISTRY AND LABORATORY MEDICINE | 2001年 / 39卷 / 03期

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

页码：281 / 282

页数：2

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