Bibliographic Details
| 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 |
