Identification of Multiple Complex Rearrangements Associated with Deletions in the 6q23-27 Region in Sézary Syndrome

Abstract

Correction to: Journal of Investigative Dermatology (2013) 133, 2617–2625; doi: 10.1038/jid.2013.188; published online 23 May 2013 Following the publication of this article, the authors noted an error in the Acknowledgments. It should read: This work was supported by the National Center of Science, Poland (KI and GKP), the German José Carreras Leukemia Foundation (PG and FCMB), and the Deutsche Forschungsgemeinschaft (CAS). The authors regret the error. Identification of Multiple Complex Rearrangements Associated with Deletions in the 6q23-27 Region in Sézary SyndromeJournal of Investigative DermatologyVol. 133Issue 11PreviewThe 6q23-27 region, recurrently deleted in Sézary syndrome (SS), was characterized at the molecular level in 13 SS patients and SS cell line SeAx. Using fine-tiling comparative genomic hybridization, deletions within the 6q23-27 region were detected in half of the samples (six patients and SeAx). All samples with deletions were further analyzed by ligation-mediated PCR. In addition, in one patient sample and in SeAx, paired-end next-generation sequencing was performed on the HiSeq2000 Illumina platform. Full-Text PDF Open Archive