Toggle Main Menu Toggle Search

Open Access padlockePrints

The Newcastle University research output collection, currently available on ePrints, will shortly be moving to a new open repository platform, Figshare. To prepare for the data migration we have paused adding new content to ePrints, and will resume once the new repository is launched. During this time you will continue to have access to ePrints (but no new content will appear). We will share updates here when available.

The natural history of infantile mitochondrial DNA depletion syndrome due to RRM2B deficiency

Lookup NU author(s): Dr Ewen Sommerville, Professor Robert TaylorORCiD

Downloads

Licence

This is the authors' accepted manuscript of an article that has been published in its final definitive form by Nature, 2020.

For re-use rights please refer to the publisher's terms and conditions.

Publication metadata

Author(s): Keshavan N, Abdenur J, Anderson G, Assouline Z, Barcia G, Bouhikbar L, Chakrapani A, Cleary M, Cohen MC, Feillet F, Fratter C, Hauser N, Jacques T, Lam A, McCullagh H, Phadke R, Rötig A, Sharrard M, Simon M, Smith C, Sommerville EW, Taylor RW, Yue WW, Rahman S

Publication type: Article

Publication status: Published

Journal: Genetics in Medicine

Year: 2020

Volume: 22

Pages: 199–209

Print publication date: 01/01/2020

Online publication date: 29/08/2019

Acceptance date: 09/07/2019

Date deposited: 17/09/2019

ISSN (print): 1098-3600

ISSN (electronic): 1530-0366

Publisher: Nature

URL: https://doi.org/10.1038/s41436-019-0613-z

DOI: 10.1038/s41436-019-0613-z

PubMed id: 31462754

Altmetrics

Altmetrics provided by Altmetric

Share