Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease.
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| Title: | Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease. |
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| Authors: | Rees, Mark I.1,2 m.i.rees@swansea.ac.uk, Harvey, Kirsten3, Pearce, Brian R.3, Seo-Kyung Chung1,2, Duguid, Ian C.4, Thomas, Philip4, Beatty, Sarah2, Graham, Gail E.5, Armstrong, Linlea6, Shiang, Rita7, Abbott, Kim J.8, Zuberi, Sameer M.9, Stephenson, John B. P.9, Owen, Michael J.10, Tijssen, Marina A. J.11, van den Maagdenberg, Arn M. J. M.12, Smart, Trevor G.4, Supplisson, Stéphane13, Harvey, Robert J.3 |
| Source: | Nature Genetics. Jul2006, Vol. 38 Issue 7, p801-806. 6p. 1 Color Photograph, 1 Diagram, 1 Chart, 2 Graphs. |
| Database: | Academic Search Ultimate |
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