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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hdl_55572.pdf | 283.16 kB | Publisher's PDF | View/Open |
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