Associated Papers
Diverse Clinical Phenotypes of CASK-Related Disorders and Multiple Functional Domains of CASK Protein.
Mori T et al.
Genes, 2023
Epilepsy-causing sequence variations in SIK1 disrupt synaptic activity response gene expression and affect neuronal morphology.
Pröschel C et al.
European Journal of Human Genetics : Ejhg, 2017
In silico prioritization based on coexpression can aid epileptic encephalopathy gene discovery.
Oliver KL et al.
Neurology. Genetics, 2016
27066588 (PubMed )
Supplement: supp_2.1.e51_table_e-2.xlsx › table_e-2
De novo mutations in SIK1 cause a spectrum of developmental epilepsies.
Hansen J et al.
American Journal of Human Genetics, 2015
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