CA Fratter, P Raman, CL Alston, EL Blakely, K Craig, C Smith, JC Evans, A Seller, B Czermin, M Hanna, J Poulton, C Brierley, T Stauton, P Turnpenny, A Schaefer, P Chinnery, R Horvath, D Turnbull, G Gorman, and R Taylor (2011)

RRM2B mutations are frequent in familial PEO with multiple mtDNA deletions

Neurology, Jun 7;76(23):2032-4.