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Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease. [electronic resource] by
- Rees, Mark I
- 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
- Stephenson, John B P
- Owen, Michael J
- Tijssen, Marina A J
- van den Maagdenberg, Arn M J M
- Smart, Trevor G
- Supplisson, Stéphane
- Harvey, Robert J
Producer: 20060911
In:
Nature genetics vol. 38
Availability: No items available.
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