Associated Papers
Evaluation of the synapse adhesion molecule Kirrel3 in neurological disease.
Shennib O et al.
Frontiers in Neurology, 2025
KIRREL3-related disorders: a case report confirming the radiological features and expanding the clinical spectrum to a less severe phenotype.
Querzani A et al.
Italian Journal of Pediatrics, 2023
A Missense De Novo Variant in the CASK-interactor KIRREL3 Gene Leading to Neurodevelopmental Disorder with Mild Cerebellar Hypoplasia.
Ciaccio C et al.
Neuropediatrics, 2021
Kirrel3-Mediated Synapse Formation Is Attenuated by Disease-Associated Missense Variants.
Taylor MR et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience, 2020
Both rare and common genetic variants contribute to autism in the Faroe Islands.
Leblond CS et al.
Npj Genomic Medicine, 2019
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