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hyperekplexia
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GLRB
The human glycine receptor beta subunit: primary structure, functional characterisation and chromosomal localisation of the human and murine genes
SLC6A5
Molecular cloning and functional expression of the human glycine transporter GlyT2 and chromosomal localisation of the gene in the human genome
GLRA1
Mutations in the alpha 1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia
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