A novel mitochondrial tRNA gene mutation causing PEO present at very low levels in skeletal muscle: implications for molecular diagnosis

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Author(s): Alston CL, Lowe J, Turnbull DM, Maddison P, Taylor RW

Publication type: Conference Proceedings (inc. Abstract)

Publication status: Published

Conference Name: Neuromuscular Disorders: 15th International Congress of the World Muscle Society

Year of Conference: 2010

Pages: 676

ISSN: 0960-8966

Publisher: Elsevier Ltd

URL: http://dx.doi.org/10.1016/j.nmd.2010.07.255

DOI: 10.1016/j.nmd.2010.07.255

Library holdings: Search Newcastle University Library for this item

ISBN: 18732364

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