Title : A critical role for glycine transporters in hyperexcitability disorders.

Pub. Date : 2008

PMID : 18946534






1 Functional Relationships(s)
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1 Recent studies of the Na(+)/Cl(-)-dependent glycine transporters GlyT1 and GlyT2 using mouse knockout models and human genetics have revealed that mutations in GlyT2 are a second major cause of hyperekplexia, while the phenotype of the GlyT1 knockout mouse resembles a devastating neurological disorder known as glycine encephalopathy (OMIM 605899). Glycine solute carrier family 6 (neurotransmitter transporter, glycine), member 9 Mus musculus