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.

Whole Exome Sequencing Reveals that Subunit Mutations are Prevalent in Complex I Deficient Leigh Syndrome

Lookup NU author(s): Professor Michael Hanna, Professor Robert TaylorORCiD, Andy Duncan

Downloads

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

Publication metadata

Author(s): Fassone E, Taanman JW, Sweeney MG, Woodward C, Hargreaves IP, Hanna MG, Taylor RW, Duncan AJ, Rahman S

Publication type: Conference Proceedings (inc. Abstract)

Publication status: Published

Conference Name: Annual Symposium of the Society for the Study of Inborn Errors of Metabolism

Year of Conference: 2012

Pages: S13-S13

ISSN: 1573-2665

Publisher: Springer

URL: http://dx.doi.org/10.1007/s10545-012-9512-z

DOI: 10.1007/s10545-012-9512-z

Series Title: Journal of Inherited Metabolic Disease

Share