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Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease / Mark Rees, Kirsten Harvey, Brian R Pearce, Seo-Kyung Chung, Ian C Duguid, Philip Thomas, Sarah Beatty, Gail E Graham, Linlea Armstrong, Rita Shiang, Kim J Abbott, Sameer M Zuberi, John B P Stephenson, Michael J Owen, Marina A J Tijssen, Trevor G Smart, Stéphane Supplisson, Robert J Harvey

Nature Genetics, Volume: 38, Issue: 7, Pages: 801 - 806

Swansea University Authors: Mark Rees, Seo-Kyung Chung

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DOI (Published version): 10.1038/ng1814

Published in: Nature Genetics
ISSN: 1061-4036
Published: 2006
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URI: https://cronfa.swan.ac.uk/Record/cronfa1441
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College: Swansea University Medical School
Issue: 7
Start Page: 801
End Page: 806