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About this Biochemistry, Genetics and Molecular Biology article
P60 Dominant and recessive RRM2B mutations cause familial PEO and multiple nit DNA deletions in muscle by C. Fratter; P. Raman; C. Alston; E.L. Blakely; K. Craig; C. Smith; J. Evans; A. Seller; B. Czermin; M.G. Hanna; J. Poulton; C. Brierley; T.G. Staunton; P.D. Turnpenny; A.M. Schaefer; P.F. Chinnery; R. Horvath; D.M. Turnbull; G.S. Gorman; R.W. Taylor is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.
- Author
- C. Fratter; P. Raman; C. Alston; E.L. Blakely; K. Craig; C. Smith; J. Evans; A. Seller; B. Czermin; M.G. Hanna; J. Poulton; C. Brierley; T.G. Staunton; P.D. Turnpenny; A.M. Schaefer; P.F. Chinnery; R. Horvath; D.M. Turnbull; G.S. Gorman; R.W. Taylor
- Publisher
- Elsevier Science; Elsevier ; Elsevier BV (ISSN 0960-8966)
- Published
- 2011
- Language
- EN
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)