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

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Title: P60 Dominant and recessive RRM2B mutations cause familial PEO and multiple nit DNA deletions in muscle
Authors: Fratter, C., Raman, P., Alston, C., 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.
Source: Neuromuscular Disorders. Mar2011 Supplement 1, Vol. 21, pS23-S23. 1p.
Database: Academic Search Ultimate
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        Value: 10.1016/S0960-8966(11)70079-7
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        Text: English
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              Text: Mar2011 Supplement 1
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