Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/55572
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Type: Journal article
Title: Mutations of the mitochondrial ND1 gene as a cause of MELAS
Author: Kirby, D.
McFarland, R.
Ohtake, A.
Dunning, C.
Ryan, M.
Wilson, C.
Ketteridge, D.
Turnbull, D.
Thorburn, D.
Taylor, R.
Citation: Journal of Medical Genetics, 2004; 41(10):784-789
Publisher: British Med Journal Publ Group
Issue Date: 2004
ISSN: 0022-2593
1468-6244
Statement of
Responsibility: 
D. M. Kirby, R. McFarland, A. Ohtake, C. Dunning, M. T. Ryan, C. Wilson, D. Ketteridge, D. M. Turnbull, D. R. Thorburn, R. W. Taylor
Keywords: Muscle, Skeletal
Cells, Cultured
Mitochondria
Fibroblasts
Humans
MELAS Syndrome
Electron Transport Complex I
NADH Dehydrogenase
DNA, Mitochondrial
DNA Mutational Analysis
Mutation
Adolescent
Child
Child, Preschool
Female
Male
Description: Copyright © 2004 by the BMJ Publishing Group Ltd. All rights reserved. BMJ Journals
DOI: 10.1136/jmg.2004.020537
Published version: http://dx.doi.org/10.1136/jmg.2004.020537
Appears in Collections:Aurora harvest 5
Paediatrics publications

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