Publication:

De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency (2003)

Author(s): McFarland R; Taylor RW; Turnbull DM; Kirby DM; Fowler KJ; Ohtake A; Ryan MT; Amor DJ; Fletcher JM; Dixon JW; Collins FA; Thorburn DR

      • Date: 4-8 November 2003
      • Conference Name: American Journal of Human Genetics: Annual Meeting of the American Society of Human Genetics
      • Volume: 73 (5)
      • Pages: 462 abstract no. 1710
      • Publisher: Cell Press
      • Publication type: Conference Proceedings (inc. abstract)
      • Bibliographic status: Published

        Keywords:

        Staff

        Professor Robert Taylor
        Professor of Mitochondrial Pathology