GLRA1Glycine Receptor Alpha 1 Subunit Gene
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References in periodicals archive ?
This condition occurs most commonly as a result of glycine receptor alpha-1 subunit gene mutation (GLRA1) in the brain and spinal nerves.
Hyperekplexia (startle disease): a novel mutation (S270T) in the M2 domain of the GLRA1 gene and a molecular review of the disorder.
A novel recessive hyperekplexia allele GLRA1 (S231R): genotyping by MALDI-TOF mass spectrometry and functional characterisation as a determinant of cellular glycine receptor trafficking.