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

      • Telephone: +44 (0) 191 208 5101

      Professor Robert Taylor
      Professor of Mitochondrial Pathology