Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Abstract Mitochondrial replacement therapies (MRTs) have been proposed as a means of avoiding the transmission of pathogenic mitochondrial DNA (mtDNA) mutations from mother to child. While clinical cases using this groundbreaking strategy have now been reported for the two principal MRT methods—pronuclear transfer and maternal spindle transfer—recent data continues to raise questions about the reliability of these approaches for disease prevention.

More information Original publication

DOI

10.1093/humrep/deag020

Type

Journal article

Publisher

Oxford University Press (OUP)

Publication Date

2026-03-08T00:00:00+00:00