Multi-disciplinary research
Publication:

RRM2B mutations are frequent in familial peo with multiple mtDNA deletions (2011)

Author(s): Fratter C, Raman P, Alston CL, 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: 01-06-2011
      • Journal: Neurology
      • Volume: 76
      • Issue: 23
      • Pages: 2032-2034
      • Publisher: Lippincott Williams & Wilkins
      • Publication type: Editorial
      • Bibliographic status: Published

      Keywords: MITOCHONDRIAL-DNA DEPLETION

      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