Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease

Rees, Mark; Harvey, Kirsten; Pearce, Brian R; Chung, Seo-Kyung; Duguid, Ian C; Thomas, Philip; Beatty, Sarah; Graham, Gail E; Armstrong, Linlea; Shiang, Rita; Abbott, Kim J; Zuberi, Sameer M; P, John B; Owen, Michael J; J, Marina A; Smart, Trevor G; Supplisson, Stéphane; Harvey, Robert J

doi:10.1038/ng1814

Journal article 1465 views

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
Online Access:	Check full text
URI:	https://cronfa.swan.ac.uk/Record/cronfa1441

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College:	Faculty of Medicine, Health and Life Sciences
Issue:	7
Start Page:	801
End Page:	806

Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease

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