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.

De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency

Lookup NU author(s): Professor Bobby McFarlandORCiD, Dr Denise Kirby, Emeritus Professor Doug Turnbull, Professor Robert TaylorORCiD

Downloads

Full text for this publication is not currently held within this repository. Alternative links are provided below where available.


Publication metadata

Author(s): McFarland R; Taylor RW; Turnbull DM; Kirby DM; Fowler KJ; Ohtake A; Ryan MT; Amor DJ; Fletcher JM; Dixon JW; Collins FA; Thorburn DR

Publication type: Conference Proceedings (inc. Abstract)

Publication status: Published

Conference Name: American Journal of Human Genetics: Annual Meeting of the American Society of Human Genetics

Year of Conference: 2003

Pages: 462 abstract no. 1710

ISSN: 0002-9297

Publisher: Cell Press

Library holdings: Search Newcastle University Library for this item

ISBN: 15376605


Share