Infantile reversible COX deficiency myopathy caused by the m.14674T &gt; C mutation in mt-tRNA(Glu) in a German family

Horvath, R; Kemp, JP; Tuppen, HAL; Hudson, G; Pyle, A; Holinski-Feder, E; Abicht, A; Czermin, B; Walter, MC; Gunther-Scholz, A; Smith, PM; McFarland, R; Chrzanowska-Lightowlers, ZMA; Lightowlers, RN; Lochmuller, H; Taylor, RW; Chinnery, PF

Infantile reversible COX deficiency myopathy caused by the m.14674T > C mutation in mt-tRNA(Glu) in a German family

Lookup NU author(s): Professor Rita Horvath ORCiD, Dr Helen Tuppen, Professor Gavin Hudson, Dr Angela Pyle, Dr Paul Smith, Professor Bobby McFarland ORCiD, Professor Zofia Chrzanowska-Lightowlers ORCiD, Professor Robert Lightowlers, Professor Hanns Lochmuller, Professor Robert Taylor, Professor Patrick Chinnery

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Author(s): Horvath R, Kemp JP, Tuppen HAL, Hudson G, Pyle A, Holinski-Feder E, Abicht A, Czermin B, Walter MC, Gunther-Scholz A, Smith PM, McFarland R, Chrzanowska-Lightowlers ZMA, Lightowlers RN, Lochmuller H, Taylor RW, Chinnery PF

Publication type: Conference Proceedings (inc. Abstract)

Publication status: Published

Conference Name: United Kingdom Neuromuscular Translational Research Conference

Year of Conference: 2010

Pages: S25-S25

ISSN: 0960-8966

Publisher: Neuromuscular Disorders, Elsevier

Library holdings: Search Newcastle University Library for this item

ISBN: 18732364

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Infantile reversible COX deficiency myopathy caused by the m.14674T > C mutation in mt-tRNA(Glu) in a German family

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