Article
RRM2B mutations are frequent in familial PEO with multiple mtDNA deletions.
Neurology - 7 Jun 2011
Fratter C, Raman P, Alston C L, Blakely E L, Craig K, Smith C, Evans J, Seller A, Czermin B, Hanna M G, Poulton J, Brierley C, Staunton T G, Turnpenny P D, Schaefer A M, Chinnery P F, Horvath R, Turnbull D M, Gorman G S, Taylor R W
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