Whole Exome Sequencing Reveals that Subunit Mutations are Prevalent in Complex I Deficient Leigh Syndrome

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Author(s): Fassone E, Taanman JW, Sweeney MG, Woodward C, Hargreaves IP, Hanna MG, Taylor RW, Duncan AJ, Rahman S

Publication type: Conference Proceedings (inc. Abstract)

Publication status: Published

Conference Name: Annual Symposium of the Society for the Study of Inborn Errors of Metabolism

Year of Conference: 2012

Pages: S13-S13

ISSN: 1573-2665

Publisher: Springer

URL: http://dx.doi.org/10.1007/s10545-012-9512-z

DOI: 10.1007/s10545-012-9512-z

Series Title: Journal of Inherited Metabolic Disease

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