Correction to: Leukemia (2009) 23, 698–707; doi:10.1038/leukemia.2008.359; published online 22 January 2009
Since the publication of this paper, the authors have noticed that part of Figure 1 has been omitted (part c). The complete figure is shown below.
Commonly deleted regions defined by array-based CGH. (a) Similar biallelic losses of 9p21 locus and chromosome 9 monosomy containing CDKN2A/CDKN2B tumour suppressor genes (blue line) in cases 2 and 3. Break points are closely located to mir-31 and mir-491 (in red). (b) Commonly deleted region located within chromosome 13 that encompasses the 13q13.3–q14.2 locus, showing a homozygous deletion of RB1 (case 9) combined with chromosome 13 partial deletion. Break points are located within RB1 (in red) and in a close vicinity of miR-16-1/miR-15a (in red). (c) Commonly deleted region located in 12p13 chromosome, involving CDKN1B and ETV6 genes (in red).
The authors would like to apologise for this error.
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The online version of the original article can be found at 10.1038/leu.2008.359
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Jardin, F., Callanan, M., Penther, D. et al. Erratum: Recurrent genomic aberrations combined with deletions of various tumour suppressor genes may deregulate the G1/S transition in CD4+CD56+ haematodermic neoplasms and contribute to the aggressiveness of the disease. Leukemia 23, 825–826 (2009). https://doi.org/10.1038/leu.2009.27
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DOI: https://doi.org/10.1038/leu.2009.27
