Specific detection of small ruminant lentiviral nucleic acid sequences located in the proviral long terminal repeat and leader-gag regions using real-time polymerase chain reaction

Author:

Brinkhof J.M.A.,van Maanen C.,Wigger R.,Peterson K.,Houwers D.J.

Publisher

Elsevier BV

Subject

Virology

Reference46 articles.

1. PCR detection of colostrum associated Maedi-Visna virus (MVV) infection and relationship with ELISA-antibody status in lambs;Álvarez;Res. Vet. Sci.,2006

2. First partial characterisation of small ruminant lentiviruses from Greece;Angelopoulou;Vet. Microbiol.,2005

3. Nucleotide sequence and biological properties of a pathogenic proviral molecular clone of neurovirulent visna virus;Andresson;Virology,1993

4. RNA-dependent DNA polymerase in virions of RNA tumour viruses;Baltimore;Nature,1970

5. Barros, S.S., Fevereiro, M.T., 2002. Cloning and sequence analysis of a Maedi Visna virus with a slow-low phenotype. NCBI Nucleotide Database, AF479638, unpublished.

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