Identification of novel and recurrent mitochondrial DNA mutations in paediatric onset mitochondrial disease using the mitochip resequencing array

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Author(s): Duncan AJ, Sweeney MG, Stern E, Taylor RW, Woodward C, Davis MB, Hanna MG, Rahman S

Publication type: Conference Proceedings (inc. Abstract)

Publication status: Published

Conference Name: Journal of Inherited Metabolic Disease: Annual Symposium of the Society for the Study of Inborn Errors of Metabolism

Year of Conference: 2008

Pages: 61 no. 242-O

ISSN: 0141-8955

Publisher: Springer Netherlands

URL: http://dx.doi.org/10.1007/s10545-008-9975-0

DOI: 10.1007/s10545-008-9975-0

Library holdings: Search Newcastle University Library for this item

ISBN: 15732665

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