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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.

Cardiomyopathy is common in patients with the mitochondrial DNA m.3243A>G mutation and correlates with mutation load

Lookup NU author(s): Dr Kieren HollingsworthORCiD, Professor Grainne Gorman, Professor Mike TrenellORCiD, Professor Bobby McFarlandORCiD, Professor Robert TaylorORCiD, Emeritus Professor Doug Turnbull, Dr Guy MacGowanORCiD, Professor Andrew BlamireORCiD, Professor Patrick Chinnery

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This is the final published version of an article that has been published in its final definitive form by Elsevier Ltd, 2012.

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

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Author(s): Hollingsworth KG, Gorman GS, Trenell MI, McFarland R, Taylor RW, Turnbull DM, Macgowan GA, Blamire AM, Chinnery PF

Publication type: Article

Publication status: Published

Journal: Neuromuscular Disorders

Year: 2012

Volume: 22

Issue: 7

Pages: 592-596

Print publication date: 16/04/2012

Date deposited: 31/10/2012

ISSN (print): 0960-8966

ISSN (electronic): 1873-2364

Publisher: Elsevier Ltd

URL: http://dx.doi.org/10.1016/j.nmd.2012.03.001

DOI: 10.1016/j.nmd.2012.03.001

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