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

Authors
Biondi, ML Marasini, B Leviti, S Turri, O Bernini, M Seminati, R Porreca, W Guagnellini, E
Citation
Ml. Biondi et al., Genotyping method for point mutation detection in the endothelial nitric oxide synthase exon 7 using fluorescent probes. Clinical validation in systemic sclerosis patients, CLIN CH L M, 39(3), 2001, pp. 281-282
Citations number
10
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
CLINICAL CHEMISTRY AND LABORATORY MEDICINE
ISSN journal
14346621 → ACNP
Volume
39
Issue
3
Year of publication
2001
Pages
281 - 282
Database
ISI
SICI code
1434-6621(200103)39:3<281:GMFPMD>2.0.ZU;2-7