Rees, MI;
Harvey, K;
Pearce, BR;
Chung, S-K;
Duguid, IC;
Thomas, P;
Beatty, S;
... Harvey, RJ; + view all
(2006)
Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease.
Nature Genetics
, 38
(7)
pp. 801-806.
10.1038/ng1814.