P60 Dominant and recessive RRM2B mutations cause familial...

Neuromuscular Disorders 2011 Vol. 21; Iss. supp-S1

P60 Dominant and recessive RRM2B mutations cause familial PEO and multiple nit DNA deletions in muscle

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.
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Volume:
21
Year:
2011
Language:
english
DOI:
10.1016/s0960-8966(11)70079-7
File:
PDF, 41 KB
english, 2011
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