Application of a simple multiplex PCR to aid in routine work of the mycobacterium reference laboratory

dc.contributor.author	Yeboah-Manu, D.
dc.contributor.author	Yates, M.D.
dc.contributor.author	Wilson, S.M.
dc.date.accessioned	2013-06-17T10:18:00Z
dc.date.accessioned	2017-10-16T13:02:16Z
dc.date.available	2013-06-17T10:18:00Z
dc.date.available	2017-10-16T13:02:16Z
dc.date.issued	2001
dc.description.abstract	A PCR specific for spacer regions 33 and 34 of the direct repeat region of the Mycobacterium tuberculosis complex was developed to complement the biochemical differentiation of M. tuberculosis, Mycobacterium bovis, M. bovis BCG, and Mycobacterium africanum subtypes I and II. In addition, this approach was incorporated into a multiplex PCR that included primers specific for IS6110 and the 65-kDa antigen gene in order to differentiate members of the M. tuberculosis complex from atypical mycobacteria.	en_US
dc.identifier.citation	Yeboah-Manu, D., Yates, M. D., & Wilson, S. M. (2001). Application of a simple multiplex PCR to aid in routine work of the mycobacterium reference laboratory. Journal of Clinical Microbiology, 39(11), 4166-4168.	en_US
dc.identifier.uri	http://197.255.68.203/handle/123456789/3262
dc.language.iso	en	en_US
dc.publisher	Journal of Clinical Microbiology	en_US
dc.title	Application of a simple multiplex PCR to aid in routine work of the mycobacterium reference laboratory	en_US
dc.type	Article	en_US

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