Associated Papers
Genetic Variant in GRM1 Underlies Congenital Cerebellar Ataxia with No Obvious Intellectual Disability.
Protasova MS et al.
International Journal of Molecular Sciences, 2023
36675067 (PubMed )
Supplement: ijms-24-01551-s001.zip › Supplemental_Table_S1.xlsx › Table_S1
The impact of Mendelian sleep and circadian genetic variants in a population setting.
Weedon MN et al.
Plos Genetics, 2022
Mutations in Metabotropic Glutamate Receptor 1 Contribute to Natural Short Sleep Trait.
Shi G et al.
Current Biology : Cb, 2021
Clustered coding variants in the glutamate receptor complexes of individuals with schizophrenia and bipolar disorder.
Frank RA et al.
Plos One, 2011
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