Journal article 1104 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
,
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
Full text not available from this repository: check for access using links below.
DOI (Published version): 10.1038/ng1814
Abstract
Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease
| Published in: | Nature Genetics |
|---|---|
| ISSN: | 1061-4036 |
| Published: |
2006
|
| Online Access: |
Check full text
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| 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 |