Publication:

Infantile reversible COX deficiency myopathy caused by the m.14674T > C mutation in mt-tRNA(Glu) in a German family (2010)

Author(s): Horvath R, Kemp JP, Tuppen HAL, Hudson G, Pyle A, Holinski-Feder E, Abicht A, Czermin B, Walter MC, Gunther-Scholz A, Smith PM, McFarland R, Chrzanowska-Lightowlers ZMA, Lightowlers RN, Lochmuller H, Taylor RW, Chinnery PF

      • Date: 25-26 March 2010
      • Conference Name: United Kingdom Neuromuscular Translational Research Conference
      • Volume: 20
      • Pages: S25-S25
      • Publisher: Neuromuscular Disorders, Elsevier
      • Publication type: Conference Proceedings (inc. abstract)
      • Bibliographic status: Published

        Keywords:

        Staff

        Professor Patrick Chinnery
        Institute Director

        Dr Gavin Hudson
        Research Fellow