Dominant and recessive RRM2B mutations cause familial PEO and multiple mtDNA deletions in muscle

Fratter, C; Raman, P; Alston, C; 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

Dominant and recessive RRM2B mutations cause familial PEO and multiple mtDNA deletions in muscle

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

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Author(s): Fratter C, Raman P, Alston C, 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: Conference Proceedings (inc. Abstract)

Publication status: Published

Conference Name: Neuromuscular Disorders: United Kingdom Neuromuscular Translational Research Conference

Year of Conference: 2011

Pages: S23

ISSN: 0960-8966

Publisher: Elsevier Ltd

Library holdings: Search Newcastle University Library for this item

ISBN: 18732364

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Dominant and recessive RRM2B mutations cause familial PEO and multiple mtDNA deletions in muscle

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