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Specific PCR primers were selected to amplify a 359 bp DNA fragment flanking the 3′-part of the polymerase gene and the 3′-noncoding (3′-NC) region of the genome of classical swine fever virus (CSFV). In RT-PCR the selected fragment was amplified from the genomes of 27 viral strains collected from Europe, America and Asia over a period of a half century as well as from three vaccine strains of CSFV...
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