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

M. L. Biondi, B. Marasini, S. Leviti, O. Turri, M. Bernini, R. Seminati, W. Porreca, E. Guagnellini

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)281-282
Number of pages2
JournalClinical Chemistry and Laboratory Medicine
Issue number3
Publication statusPublished - 2001


  • Fluorescent probes
  • NO-synthase exon 7 polymorphism
  • Systemic sclerosis

ASJC Scopus subject areas

  • Clinical Biochemistry

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