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



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

      Professor Robert Taylor
      Professor of Mitochondrial Pathology

      Professor Doug Turnbull
      Professor of Neurology