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Mitochondrial Replacement Therapy and Identity: A Comment on an Exchange Between Inmaculada de Melo-Martin and John Harris

Published online by Cambridge University Press:  30 May 2018

SØREN HOLM
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Information
Cambridge Quarterly of Healthcare Ethics , Volume 27 , Issue 3 , July 2018 , pp. 487 - 491
Copyright
Copyright © Cambridge University Press 2018 

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References

Notes

1. de Melo-Martín, I. When the milk of human kindness becomes a luxury (and untested) good. Cambridge Quarterly of Healthcare Ethics. 2017;26(1):159–65.Google Scholar

2. Harris, J. How to welcome new technologies: some comments on the article by Inmaculada de Melo-Martin. Cambridge Quarterly of Healthcare Ethics 2017;26(1):166–72.CrossRefGoogle Scholar

3. Harris, J. Germline modification and the burden of human existence. Cambridge Quarterly of Healthcare Ethics 2016;25(1):6–18.Google Scholar

4. See note 1, de Melo-Martín 2017, at 160.

5. See note 2, Harris 2017, at 166–7.

6. See note 3, Harris 2016, at 11.

7. Parfit, D. Reasons and Persons. Oxford: Oxford University Press; 1986.Google Scholar

8. Tuppen, HA, Blakely, EL, Turnbull, DM, Taylor, RW. Mitochondrial DNA mutations and human disease. Biochimica et Biophysica Acta 2010;1797(2):113–28, at 117.CrossRefGoogle ScholarPubMed

9. I owe this argument to Iain Brassington.

10. See note 8, Tuppen et al. 2010, at 117.

11. Schapira AH. Mitochondrial disease. The Lancet 2006;368(9529):70–82.

12. See note 3, Harris 2016.

13. Nuffield Council on Bioethics. Novel Techniques for the Prevention of Mitochondrial DNA Disorders: An Ethical Review. London: Nuffield Council on Bioethics; 2012, at 53.

14. See note 2, Harris 2017.

15. See note 3, Harris 2016.