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

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Description scientific article
Author/s

author: Seo-Kyung Chung  Mark I Rees  Marina A. J. Tijssen  Sameer M Zuberi  Trevor G Smart  Linlea Armstrong  Robert J. Harvey  Ian C Duguid  Arn van den Maagdenberg 

Publication date June 4, 2006
Language English
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