Recurrent mutations in the NDUFS2 gene causing isolated complex I deficiency in skeletal muscle

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

Author(s): McFarland R, Tuppen H, He L, Blakely EL, Morris AAM, Clarke M, Jones S, Devlin AM, Taylor RW

Publication type: Conference Proceedings (inc. Abstract)

Publication status: Published

Conference Name: Neuromuscular Disorders: 14th International Congress of the World Muscle Society

Year of Conference: 2009

Pages: 562

ISSN: 0960-8966

Publisher: Elsevier Ltd

URL: http://dx.doi.org/10.1016/j.nmd.2009.06.061

DOI: 10.1016/j.nmd.2009.06.061

Library holdings: Search Newcastle University Library for this item

ISBN: 18732364

ePrints