Newcastle University

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

• URL: http://dx.doi.org/10.1212/WNL.0b013e31821e558b
• DOI: 10.1212/WNL.0b013e31821e558b
• ISSN (electronic): 1526-632X

Keywords: MITOCHONDRIAL-DNA DEPLETION

Staff

Professor Patrick Chinnery Wellcome Senior Fellow in Clinical Science, Professor of Neurogenetics and Honorary Consultant	Email: patrick.chinnery@ncl.ac.uk Telephone: +44 (0) 191 222 5101
Dr Grainne Gorman Biomedical Research Centre Fellow	Email: grainne.gorman@ncl.ac.uk Telephone: +44 (0) 191 222 6365
Professor Robert Taylor Professor of Mitochondrial Pathology	Email: robert.taylor@ncl.ac.uk Telephone: +44 (0) 191 222 3685
Professor Doug Turnbull Professor of Neurology	Email: doug.turnbull@ncl.ac.uk Telephone: +44 (0) 191 222 8334