data from the present study suggest a possible role of GABRQ rs3810651 single nucleotide polymorphism in the modification of the age at onset of migraine in the Caucasian Spanish people
We identified truncating mutations in distinct X-linked gamma-aminobutyric acid A (GABAA) receptor subunit-encoding genes GABRQ and GABRA3.this is the first report of ASD patients with truncating mutations in GABA receptors genes.
Observational study of gene-disease association. (HuGE Navigator); Although GABRQ genes did not show positive association further studies are necessary to consider the role of other GABA receptor genes in migraine susceptibility
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