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. Green open access