Genotyping Method for Point Mutation Detection in the Endothelial Nitric Oxide Synthase Exon 7 Using Fluorescent Probes. Clinical Validation in Systemic Sclerosis Patients
Gespeichert in:
Verfasser / Beitragende:
[Maria L. Biondi, Bianca Marasini, Simona Leviti, Olivia Turri, Mara Bernini, Raffaella Seminati, Wanda Porreca, Emma Guagnellini]
Ort, Verlag, Jahr:
2001
Enthalten in:
Clinical Chemistry and Laboratory Medicine, 39/3(2001-04-09), 281-282
Format:
Artikel (online)
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