Multi-disciplinary research
Publication:

Dominant and recessive RRM2B mutations cause familial PEO and multiple mtDNA deletions in muscle (2011)

Author(s): Fratter C, Raman P, Alston C, Blakely EL, Craig K, Smith C, Evans J, Seller A, Czermin B, Hanna MG, Poulton J, Brierley C, Staunton TG, Turnpenny PD, Schaefer AM, Chinnery PF, Horvath R, Turnbull DM, Gorman GS, Taylor RW

      • Date: 29-30 March 2011
      • Conference Name: Neuromuscular Disorders: United Kingdom Neuromuscular Translational Research Conference
      • Volume: 21 (s1)
      • Pages: S23
      • Publisher: Elsevier Ltd
      • Publication type: Conference Proceedings (inc. abstract)
      • Bibliographic status: Published

        Keywords:

        Staff

        Professor Patrick Chinnery
        Wellcome Senior Fellow in Clinical Science, Professor of Neurogenetics and Honorary Consultant

        Dr Grainne Gorman
        Biomedical Research Centre Fellow

        Professor Robert Taylor
        Professor of Mitochondrial Pathology

        Professor Doug Turnbull
        Professor of Neurology