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Number of items: 4.

Hunt, D.M. and Wilkie, S.E. and Newbold, R. and Deery, E. and Warren, M.J. and Bhattacharya, S.S. and Zhang, K. (2004) Dominant cone and cone-rod dystrophies: functional analysis of mutations in retGC1 and GCAP1. In: Bock, G. and Chader, G. and Goode, J., eds. Retinal Dystrophies: Functional Genomics to Gene Therapy. Novartis Foundation Symposia, 255 . John Wiley & Sons, pp. 37-49. ISBN 9780470853573. (The full text of this publication is not available from this repository)

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)

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)

Sokal, I. and Li, N. and Surgucheva, I. and Warren, M.J. and Payne, A.M. and Bhattacharya, S.S. and Baehr, W. and Palczewski, K. (1998) GCAP1 (Y99C) mutant is constitutively active in autosomal dominant cone dystrophy. Molecular Cell, 2 (1). pp. 129-33. ISSN 1097-2765 . (The full text of this publication is not available from this repository)

This list was generated on Mon Apr 21 00:51:01 2014 BST.