Rapid detection of equine infectious anaemia virus nucleic acid by insulated isothermal RT ‐ PCR assay to aid diagnosis under field conditions

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Niaz Banaei

By targeting theerm(41) andrrlgenes in theMycobacterium abscessusgroup, a multiplex real-time PCR assay for clarithromycin resistance showed 95% (38/40) concordance with nucleic acid testing and 95% (37/39) concordance with phenotypic testing. This assay provides a simple and rapid alternative to extended incubation orerm(41) sequencing.



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