RRM2B mutations are frequent in familial peo with multiple mtDNA deletions

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

doi:10.1212/WNL.0b013e31821e558b

RRM2B mutations are frequent in familial peo with multiple mtDNA deletions

Lookup NU author(s): Dr Andrew Schaefer, Professor Patrick Chinnery, Professor Rita Horvath ORCiD, Emeritus Professor Doug Turnbull, Professor Grainne Gorman, Professor Robert Taylor

Downloads

Full text for this publication is not currently held within this repository. Alternative links are provided below where available.

Publication metadata

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

Publication type: Editorial

Publication status: Published

Journal: Neurology

Year: 2011

Volume: 76

Issue: 23

Pages: 2032-2034

Print publication date: 01/06/2011

ISSN (print): 0028-3878

ISSN (electronic): 1526-632X

Publisher: Lippincott Williams & Wilkins

URL: http://dx.doi.org/10.1212/WNL.0b013e31821e558b

DOI: 10.1212/WNL.0b013e31821e558b

ePrints

RRM2B mutations are frequent in familial peo with multiple mtDNA deletions

Downloads

Publication metadata

Share