1996
DOI: 10.1016/0168-1702(96)01312-3
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Geographic distribution and epidemiology of peste des petits ruminants viruses

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Cited by 239 publications
(218 citation statements)
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“…However, this assay may not always be suitable for diagnosis of every virus strain, variant or isolate, as changes at the 3 0 end of the primer binding sites, as a result of variation between strains in the immunogenic protein coding region, may yield a false-negative result. A two-step RT-PCR has been shown to useful for the rapid detection of virus specific RNA in the samples submitted for laboratory diagnosis [35,57,128]. Further, PCR strategies targeting M and N gene have been developed for detection and differentiation of PPRV in sheep and goats.…”
Section: Polymerase Chain Reactionmentioning
confidence: 99%
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“…However, this assay may not always be suitable for diagnosis of every virus strain, variant or isolate, as changes at the 3 0 end of the primer binding sites, as a result of variation between strains in the immunogenic protein coding region, may yield a false-negative result. A two-step RT-PCR has been shown to useful for the rapid detection of virus specific RNA in the samples submitted for laboratory diagnosis [35,57,128]. Further, PCR strategies targeting M and N gene have been developed for detection and differentiation of PPRV in sheep and goats.…”
Section: Polymerase Chain Reactionmentioning
confidence: 99%
“…Due to improved understanding of the viral genome and molecular biological techniques, nucleic acid-based specific and sensitive assays were also developed [41,43,105,128].…”
Section: Molecular Diagnostic Techniquesmentioning
confidence: 99%
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