RRM2B mutations are frequent in familial peo with multiple mtDNA deletions

Dr Andrew Schaefer; Professor Patrick Chinnery; Dr Rita Horvath; Professor Doug Turnbull; Dr Grainne Gorman; Professor Robert Taylor

RRM2B mutations are frequent in familial peo with multiple mtDNA deletions Lookup NU author(s) Dr Andrew Schaefer Professor Patrick Chinnery Dr Rita Horvath Professor Doug Turnbull Dr Grainne Gorman Professor Robert Taylor



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
Journal		Neurology
Year		2011
Volume		76
Issue		23
Pages		2032-2034
ISSN (print)		0028-3878
ISSN (electronic)		1526-632X



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Publisher		Lippincott Williams & Wilkins
URL		http://dx.doi.org/10.1212/WNL.0b013e31821e558b
DOI		10.1212/WNL.0b013e31821e558b

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