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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

M.A. Maw

Department of Biochemistry

University of Otago


New Zealand


Name/email consistency: high



  • Department of Biochemistry, University of Otago, Dunedin, New Zealand. 1997 - 2000


  1. 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) [Pubmed]
  2. 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) [Pubmed]
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