Funding sources None.
Clinical and Laboratory Investigations
Rapid detection of HLA-A*31:01 allele in DNA and blood samples using loop-mediated isothermal amplification
Version of Record online: 18 JUN 2014
© 2014 British Association of Dermatologists
British Journal of Dermatology
Volume 171, Issue 1, pages 90–96, July 2014
How to Cite
Cheung, Y.K., Kwok, M., Chan, E. and Kwan, P. (2014), Rapid detection of HLA-A*31:01 allele in DNA and blood samples using loop-mediated isothermal amplification. British Journal of Dermatology, 171: 90–96. doi: 10.1111/bjd.12897
Conflicts of interest P.K. has provided consultancy services to Eisai, GSK, Pfizer and UCB Pharma, received research support from Eiasi, Johnson & Johnson, Pfizer and UCB Pharma, and lectured in speakers' bureaus of Eisai and UCB Pharma. The other authors have no conflicts of interest to declare.
- Issue online: 26 JUL 2014
- Version of Record online: 18 JUN 2014
- Accepted manuscript online: 5 MAR 2014 03:36AM EST
- Manuscript Accepted: 10 FEB 2014
- Johnson & Johnson
- UCB Pharma
|bjd12897-sup-0001-TableS1.docx||Word document||42K||Table S1 HLA-A*31:01 testing results from the loop-mediated isothermal amplification-based protocol compared with the known HLA-A genotypes in genomic DNA samples derived from B-cell lines (n = 66).|
|bjd12897-sup-0002-TableS2.docx||Word document||39K||Table S2 HLA-A*31:01 testing results from the loop-mediated isothermal amplification-based protocol compared with those from sequence-based typing in blood and extracted DNA samples collected from patients with epilepsy (n = 34). Testing on both DNA and blood samples showed the same results.|
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