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
      Institute Director