The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple families
Helen AL Tuppen, Vanessa E Hogan, Langping He, Emma L Blakely, Lisa Worgan, Mazhor Al-Dosary, Gabriele Saretzki, Charlotte L Alston, Andrew A Morris, Michael Clarke, Simon Jones, Anita M Devlin, Sahar Mansour, Zofia MA Chrzanowska-Lightowlers, David R Thorburn, Robert McFarland, Robert W Taylor
Brain | OXFORD UNIV PRESS | Published : 2010
Awarded by Wellcome Trust
Awarded by Medical Research Council
Wellcome Trust Programme Grant (074454/Z/04/Z; to Z.M.A. C-L. and R. W. T.); the Newcastle upon Tyne Hospitals NHS Foundation Trust Special Trustees; United Kingdom National Commissioning Group 'Rare Mitochondrial Disorders of Adults and Children' Diagnostic Service (http://www.mitochondrialncg.nhs.uk); Australian National Health and Medical Research Council Principal Research Fellowship (to D. R. T.).