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. 2016 Oct 7;30(12):2430. doi: 10.1038/leu.2016.237

Erratum: Comprehensive mutational analysis of primary and relapse acute promyelocytic leukemia

V Madan, P Shyamsunder, L Han, A Mayakonda, Y Nagata, J Sundaresan, D Kanojia, K Yoshida, S Ganesan, N Hattori, N Fulton, K T Tan, T Alpermann, M C Kuo, S Rostami, J Matthews, M Sanada, L-Z Liu, Y Shiraishi, S Miyano, E Chendamarai, H A Hou, G Malnassy, T Ma, M Garg, L W Ding, Q Y Sun, W Chien, T Ikezoe, M Lill, A Biondi, R A Larson, B L Powell, M Lübbert, W J Chng, H F Tien, M Heuser, A Ganser, M Koren-Michowitz, S M Kornblau, H M Kantarjian, D Nowak, W K Hofmann, H Yang, W Stock, A Ghavamzadeh, K Alimoghaddam, T Haferlach, S Ogawa, L Y Shih, V Mathews, H P Koeffler
PMCID: PMC7609306  PMID: 27713533

Correction to: Leukemia (2016) 30, 1672–1681; doi:10.1038/leu.2016.69

Following the publication of this article, the authors have noted that three genes: FLT3, NRAS and ARID1A (each with mutational frequency of 5%) have been incorrectly labelled in Figure 4a showing the mutational landscape of APL relapse.

Figure 4.

Figure 4

Spectrum of somatic mutations at APL relapse. (a) Matrix displays top 15 genes recurrently mutated at relapsed APL. Each column represents a relapse sample. Genes are arranged according to decreasing mutational frequencies from top to bottom. Right panel illustrates the number of mutations for all genes. Only those relapse samples that harbor mutations of top 15 genes are included in the matrix.

Below is the corrected figure.

The authors confirm that the above mislabeling has no impact on the conclusions made and wish to apologize for any inconvenience caused.

Footnotes

The online version of the original article can be found at 10.1038/leu.2016.69


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