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Number of items: 2.

2002

Deery, E.C. and Vithana, E.N. and Newbold, R.J. and Gallon, V.A. and Bhattacharya, S.S. and Warren, M.J. and Hunt, D.M. and Wilkie, S.E. (2002) Disease mechanism for retinitis pigmentosa (RP11) caused by mutations in the splicing factor gene PRPF31. human molecular genetics, 11 (25). pp. 3209-3219. ISSN 0964-6906 . (The full text of this publication is not available from this repository)

2001

Wilkie, S.E. and Li, Y. and Deery, E.C. and Newbold, R.J. and Garibaldi, D. and Bateman, J.B. and Zhang, H. and Lin, W. and Zack, D.J. and Bhattacharya, S.S. and Warren, M.J. and Hunt, D.M. and Zhang, K. (2001) Identification and functional consequences of a new mutation (E155G) in the gene for GCAP1 that causes autosomal dominant cone dystrophy. American Journal Humman Genetics, 69 (3). pp. 471-80. ISSN 0002-9297 . (The full text of this publication is not available from this repository)

This list was generated on Thu Apr 24 08:53:12 2014 BST.