M.A. Maw
Department of Biochemistry
University of Otago
Dunedin
New Zealand
Name/email consistency: high
- A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration. Maw, M.A., Corbeil, D., Koch, J., Hellwig, A., Wilson-Wheeler, J.C., Bridges, R.J., Kumaramanickavel, G., John, S., Nancarrow, D., Röper, K., Weigmann, A., Huttner, W.B., Denton, M.J. Hum. Mol. Genet. (2000)
- Mutation of the gene encoding cellular retinaldehyde-binding protein in autosomal recessive retinitis pigmentosa. Maw, M.A., Kennedy, B., Knight, A., Bridges, R., Roth, K.E., Mani, E.J., Mukkadan, J.K., Nancarrow, D., Crabb, J.W., Denton, M.J. Nat. Genet. (1997)
