Genotyping Method for Point Mutation Detection in the Endothelial Nitric Oxide Synthase Exon 7 Using Fluorescent Probes. Clinical Validation in Systemic Sclerosis Patients
- 9 January 2001
- journal article
- Published by Walter de Gruyter GmbH in cclm
- Vol. 39 (3) , 281-282
- https://doi.org/10.1515/cclm.2001.043
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
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