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Number of items: 2.

Article

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.

Book section

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.

This list was generated on Thu Jun 20 03:21:35 2013 BST.