Recurrent mutations in the NDUFS2 gene causing isolated complex I deficiency in skeletal muscle
- Lookup NU author(s)
- Dr Bobby McFarland
- Dr Helen Tuppen
- Dr Andrew Morris
- Dr Anita Devlin
- Professor Robert Taylor
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| Author(s) | | McFarland R, Tuppen H, He L, Blakely EL, Morris AAM, Clarke M, Jones S, Devlin AM, Taylor RW |
| Editor(s) | | |
| Publication type | | Conference Proceedings (inc. Abstract) |
| Conference Name | | Neuromuscular Disorders: 14th International Congress of the World Muscle Society |
| Conference Location | | Geneva, Switzerland |
| Year of Conference | | 2009 |
| Date | | 9-12 September 2009 |
| Volume | | 19, 8-9 |
| Pages | | 562 |
| | 0960-8966 |
| ISBN | | 18732364 |
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| Full text for this publication is not currently held within this repository. Alternative links are provided below where available. |
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| Publisher | | Elsevier Ltd |
| URL | | http://dx.doi.org/10.1016/j.nmd.2009.06.061 |
| DOI | | 10.1016/j.nmd.2009.06.061 |
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