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Rees, M.I., Harvey, K., Chung, S-K., Duguid, I.C., Thomas, P., Beatty, S., Graham, G., Armstrong, L., Shiang, R., Abbott, K.J., Zuberi, S., Stephenson, S., Owen, M.J., Tijssen, M.A.J., van den Maagdenberg, A.M.J.M., Smart, T.G., Supplisson, S. and Harvey, R.J. (2006) Mutations in the human GlyT2 gene define a presynaptic component of human startle disease. Nature Genetics, 38 . pp. 801-806. 10.1038/ng1814.

Rees, M.I., Harvey, K., Pearce, B.R., Chung, S-K., Duguid, I.C., Thomas, P., Beatty, S., Graham, G.E., Armstrong, L., Shiang, R., Abbott, K.J., Zuberi, S.M., Stephenson, J.B.P., Owen, M.J., Tijssen, M.A.J., van den Maagdenberg, A.M.J.M., Smart, T.G., Supplisson, S. and Harvey, R.J. (2006) Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease. Nature Genetics, 38 (7). pp. 801-806. 10.1038/ng1814.

This list was generated on Thu Aug 28 02:01:23 2014 BST.