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The Journal of Medical Microbiology, Vol 42, Issue 5 367-371, Copyright © 1995 by Society for General Microbiology
JOURNAL ARTICLE |
A. Karachristos, S. Linardopoulos, M. Ergazaki and D. A. Spandidos
Laboratory of Clinical Virology, Medical School, University of Crete, Heraklion, Greece.
A combined reverse transcription-polymerase chain reaction (RT-PCR) method was employed for the detection of hepatitis C virus (HCV) RNA in serum from patients with chronic active hepatitis, with primers corresponding to the 5' non-coding region. The diagnosis was based on serological and biochemical methods and on liver biopsy. HCV-RNA was detected in 27 (90%) of 30 sera examined. The nucleotide sequence of PCR-amplified HCV cDNAs (256 bp) was determined from five specimens and heterogeneity varying between 0.58% and 2.89% among the clinical samples and the prototype HCV-1 was found.
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