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Erratum to: Brain Tumor Pathol (2015) 32:22–30 DOI 10.1007/s10014-014-0186-0
In original publication of article, the pyrosequencing assay for IDH2 in Table 1 was incorrectly described as follows:
Sequence to analyze: ANGCAC.
Dispensation order: TATGTCACGCAC.
The correct assay is as follows:
Sequence to analyze: ANGCACGCCCAT.
Dispensation order: GTACTGTCACGC.
The corrected version of Table 1 is given in this erratum.
In addition, the authors would like to include the below comment with this erratum.
Another point which we would like to comment on is about R172S mutation, an extremely rare mutation in IDH2 for gliomas. Two types of single nucleotide change have been reported as an R172S mutation (c.516G>C and c.516G>T) [1, 2]. In the present study, we validated the assay for IDH2 using a plasmid generated from a clinical case with c.516G>T transition (Fig. 1). Theoretically, the other R172S mutation (c.516G>C) would also be detected by increased peaks at the 6th (G) and 8th (C) dispensations. This type of mutation is extremely rare in gliomas, and our assays are still useful in detecting either mutation.
References
Horbinski C (2013) What do we know about IDH1/2 mutations so far, and how do we use it? Acta Neuropathol (Berl) 125:621–636
Sonoda Y, Kumabe T, Nakamura T, Saito R, Kanamori M, Yamashita Y, Suzuki H, Tominaga T (2009) Analysis of IDH1 and IDH2 mutations in Japanese glioma patients. Cancer Sci 100:1996–1998
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The online version of the original article can be found at https://doi.org/10.1007/s10014-014-0186-0.
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Arita, H., Narita, Y., Matsushita, Y. et al. Erratum to: Development of a robust and sensitive pyrosequencing assay for the detection of IDH1/2 mutations in gliomas. Brain Tumor Pathol 35, 46–47 (2018). https://doi.org/10.1007/s10014-017-0277-9
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DOI: https://doi.org/10.1007/s10014-017-0277-9