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How to find us dr. D.R.M. Vlaskamp, BSc

Publications

GRIN2A-related disorders: genotype and functional consequence predict phenotype

PRRT2-related phenotypes in patients with a 16p11.2 deletion

Schizophrenia is a later-onset feature of PCDH19 Girls Clustering Epilepsy

SYNGAP1 encephalopathy: A distinctive generalized developmental and epileptic encephalopathy

Genotyping and phenotyping epilepsies of childhood

SYNGAP1 Developmental and Epileptic Encephalopathy: Delineating the Phenotypic Spectrum

Copy number variation in a hospital-based cohort of children with epilepsy

Haploinsufficiency of the STX1B gene is associated with myoclonic astatic epilepsy

Variable phenotypes in individuals with grin2a sequence variants or deletions

Copy number variants in a hospital-based cohort of children with epilepsy

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