Mutations in the human GlyT2 gene define a presynaptic component of human startle disease

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.

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DOI: 10.1038/ng1814


Item Type:Article
Departments, units and centres:Department of Pharmacology > Department of Pharmacology
ID Code:74
Journal or Publication Title:Nature Genetics
Deposited By:Library Staff
Deposited On:03 Aug 2006
Last Modified:31 Mar 2011 11:31

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