dc.contributor.author |
Byaruhanga, Charles
|
|
dc.contributor.author |
Makgabo, Sekgota Marcus
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|
dc.contributor.author |
Choopa, Chimvwele Namantala
|
|
dc.contributor.author |
Mulandane, Fernando C.
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|
dc.contributor.author |
Vorster, Ilse
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|
dc.contributor.author |
Troskie, Milana
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|
dc.contributor.author |
Chaisi, Mamohale E.
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|
dc.contributor.author |
Collins, Nicola E.
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|
dc.date.accessioned |
2024-01-15T12:56:11Z |
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dc.date.available |
2024-01-15T12:56:11Z |
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dc.date.issued |
2023-03 |
|
dc.description |
DATA AVAILABILITY : Data will be made available on request. |
en_US |
dc.description.abstract |
Please read abstract in the article. |
en_US |
dc.description.department |
Veterinary Tropical Diseases |
en_US |
dc.description.librarian |
am2024 |
en_US |
dc.description.sdg |
SDG-03:Good heatlh and well-being |
en_US |
dc.description.uri |
https://www.elsevier.com/locate/ttbdis |
en_US |
dc.identifier.citation |
Byaruhanga, C., Makgabo, S.M., Choopa, C.N. et al. 2023, 'Genetic diversity in Babesia bovis from southern Africa and estimation of B. bovis infection levels in cattle using an optimised quantitative PCR assay', Ticks and Tick-borne Diseases, vol. 14, art. 102084, pp. 1-9. https://DOI.org/10.1016/j.ttbdis.2022.102084. |
en_US |
dc.identifier.issn |
1877-959X |
|
dc.identifier.other |
10.1016/j.ttbdis.2022.102084 |
|
dc.identifier.uri |
http://hdl.handle.net/2263/93962 |
|
dc.language.iso |
en |
en_US |
dc.publisher |
Elsevier |
en_US |
dc.rights |
© 2023 The Authors. Published by Elsevier GmbH. This is an open access article under the CC BY-NC-ND license. |
en_US |
dc.subject |
18S rRNA |
en_US |
dc.subject |
msa-2b |
en_US |
dc.subject |
Real-time PCR |
en_US |
dc.subject |
Quantification |
en_US |
dc.subject |
Reverse line blot |
en_US |
dc.subject |
Quantitative real-time PCR (qPCR) |
en_US |
dc.subject |
South Africa (SA) |
en_US |
dc.subject |
SDG-03: Good health and well-being |
en_US |
dc.title |
Genetic diversity in Babesia bovis from southern Africa and estimation of B. bovis infection levels in cattle using an optimised quantitative PCR assay |
en_US |
dc.type |
Article |
en_US |