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

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Mark I. Rees

School of Medicine

University of Wales Swansea

Singleton Park

West Glamorgan SA2 8PP

[email]@swansea.ac.uk

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Affiliation

School of Medicine, University of Wales Swansea, Singleton Park, West Glamorgan SA2 8PP, UK. 2006

References

Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease. 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., Owen, M.J., Tijssen, M.A., van den Maagdenberg, A.M., Smart, T.G., Supplisson, S., Harvey, R.J. Nat. Genet. (2006) [Pubmed]