Mark I. Rees
Department of Molecular Medicine
University of Auckland Medical School
Postbag 92019
Auckland
New Zealand
Name/email consistency: high
- Isoform heterogeneity of the human gephyrin gene (GPHN), binding domains to the glycine receptor, and mutation analysis in hyperekplexia. Rees, M.I., Harvey, K., Ward, H., White, J.H., Evans, L., Duguid, I.C., Hsu, C.C., Coleman, S.L., Miller, J., Baer, K., Waldvogel, H.J., Gibbon, F., Smart, T.G., Owen, M.J., Harvey, R.J., Snell, R.G. J. Biol. Chem. (2003)
- Compound heterozygosity and nonsense mutations in the alpha(1)-subunit of the inhibitory glycine receptor in hyperekplexia. Rees, M.I., Lewis, T.M., Vafa, B., Ferrie, C., Corry, P., Muntoni, F., Jungbluth, H., Stephenson, J.B., Kerr, M., Snell, R.G., Schofield, P.R., Owen, M.J. Hum. Genet. (2001)
- Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA3). Rees, M.I., Watts, P., Fenton, I., Clarke, A., Snell, R.G., Owen, M.J., Gray, J. Hum. Genet. (2000)