A GRM7 mutation associated with developmental delay reduces mGlu7 expression and produces neurological phenotypes.

Fisher NM, AlHashim A, Buch AB, Badivuku H, Samman MM, Weiss KM, Cestero GI, Does MD, Rook JM, Lindsley CW, Conn PJ, Gogliotti RG, Niswender CM
JCI Insight. 2021 6 (4)

PMID: 33476302 · PMCID: PMC7934925 · DOI:10.1172/jci.insight.143324

MeSH Terms (21)

Animals Autism Spectrum Disorder Child Child, Preschool Epilepsy Fear Female Genetic Predisposition to Disease GTP-Binding Proteins Humans Infant Learning Male Mice Mice, Inbred C57BL Mutation Neurodevelopmental Disorders Pedigree Phenotype Receptors, Metabotropic Glutamate Seizures

Connections (3)

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