Erratum to non-homologous end-joining protein expression screen from radiosensitive cancer patients yields a novel DNA double strand break repair phenotype
Erratum

Erratum to non-homologous end-joining protein expression screen from radiosensitive cancer patients yields a novel DNA double strand break repair phenotype

Michael J. McKay1, Su Kah Goh2, Jeremy N. McKay3, Michael Chao4, Timothy M. McKay5

1University of Sydney, Department of Medicine, Camperdown, 2050 NSW, Australia;2Peter MacCallum Cancer Centre, Melbourne, VIC, Australia;3Monash University, Clayton, 3260 VIC, Australia;4Genesis Cancer Care, Melbourne, 3001 VIC, Australia;5Deakin University, Burwood, 3125 VIC, Australia

Correspondence to: Professor Michael J. McKay. University of Sydney, Department of Medicine, Camperdown, 2050 NSW, Australia. Email: cohesin@yahoo.com.au.

doi: 10.21037/atm.2017.07.33


Erratum to: Ann Transl Med 2017;5:96

Non-homologous end-joining protein expression screen from radiosensitive cancer patients yields a novel DNA double strand break repair phenotype

In the article entitled “Non-homologous end-joining protein expression screen from radiosensitive cancer patients yields a novel DNA double strand break repair phenotype” (1) that appeared on Page 96 of Vol 5, No 5 of Annals of Translational Medicine, there was an error. The author’s name “Su Kak Goh” should be corrected as “Su Kah Goh”.

In addition, the new affiliation of Dr. Su Kah Goh is “Department of Surgery, The University of Melbourne, Austin Health, VIC, Australia”.

We are sorry for the inconvenience caused.


References

  1. McKay MJ, Goh SK, McKay JN, et al. Non-homologous end-joining protein expression screen from radiosensitive cancer patients yields a novel DNA double strand break repair phenotype. Ann Transl Med 2017;5:96. [Crossref] [PubMed]
Cite this article as: McKay MJ, Goh SK, McKay JN, Chao M, McKay TM. Erratum to non-homologous end-joining protein expression screen from radiosensitive cancer patients yields a novel DNA double strand break repair phenotype. Ann Transl Med 2017;5(15):318. doi: 10.21037/atm.2017.07.33

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