Background: Heterozygous copy number variants (CNVs) or sequence variants in the contactin-associated protein 2 gene CNTNAP2 have been discussed as risk factors for a wide spectrum of neurodevelopmental and neuropsychiatric disorders. Bi-allelic aberrations in this gene are causative for an autosomal-recessive disorder with epilepsy, severe intellectual disability (ID) and cortical dysplasia (CDFES). As the number of reported individuals is still limited, we aimed at a further characterisation of the full mutational and clinical spectrum. Methods: Targeted sequencing, chromosomal microarray analysis or multigene panel sequencing was performed in individuals with severe ID and epilepsy. Results: We identified homozygous mutations, compound h...
Epilepsy is one of the most common neurological disorders in humans with a prevalence of 1% and a li...
Epilepsy is one of the most common neurological disorders in humans with a prevalence of 1% and a li...
Background Copy number variants (CNVs) have been linked to neurodevelopmental disorders such as inte...
Background Heterozygous copy number variants (CNVs) or sequence variants in the contactin-associated...
BACKGROUND : Heterozygous copy number variants (CNVs) or sequence variants in the contactin-associat...
BACKGROUND: Heterozygous copy-number and missense variants in CNTNAP2 and NRXN1 have repeatedly been...
Background: Heterozygous mutations in CNTNAP2 have been identified in patients with a range of compl...
Abbreviations: ID (Intellectual disability), ASD (autism spectrum disorder), SCZ (schizophrenia), BD...
Contactin-associated protein-like 2 (CNTNAP2) gene encodes for CASPR2, a presynaptic type 1 transmem...
The genetic basis of complex neurological disorders involving language are poorly understood, partly...
Background: Heterozygous variants in CNTNAP2 have been implicated in a wide range of neurological ph...
Background: Heterozygous variants in CNTNAP2 have been implicated in a wide range of neurological p...
Introduction: Mutations in the contactin-associated protein-like 2 (CNTNAP2) gene (MIM#604569) encod...
International audienceThe CNTNAP2 gene has been proposed to be one of the major susceptibility genes...
Epilepsy is one of the most common neurological disorders in humans with a prevalence of 1% and a li...
Epilepsy is one of the most common neurological disorders in humans with a prevalence of 1% and a li...
Background Copy number variants (CNVs) have been linked to neurodevelopmental disorders such as inte...
Background Heterozygous copy number variants (CNVs) or sequence variants in the contactin-associated...
BACKGROUND : Heterozygous copy number variants (CNVs) or sequence variants in the contactin-associat...
BACKGROUND: Heterozygous copy-number and missense variants in CNTNAP2 and NRXN1 have repeatedly been...
Background: Heterozygous mutations in CNTNAP2 have been identified in patients with a range of compl...
Abbreviations: ID (Intellectual disability), ASD (autism spectrum disorder), SCZ (schizophrenia), BD...
Contactin-associated protein-like 2 (CNTNAP2) gene encodes for CASPR2, a presynaptic type 1 transmem...
The genetic basis of complex neurological disorders involving language are poorly understood, partly...
Background: Heterozygous variants in CNTNAP2 have been implicated in a wide range of neurological ph...
Background: Heterozygous variants in CNTNAP2 have been implicated in a wide range of neurological p...
Introduction: Mutations in the contactin-associated protein-like 2 (CNTNAP2) gene (MIM#604569) encod...
International audienceThe CNTNAP2 gene has been proposed to be one of the major susceptibility genes...
Epilepsy is one of the most common neurological disorders in humans with a prevalence of 1% and a li...
Epilepsy is one of the most common neurological disorders in humans with a prevalence of 1% and a li...
Background Copy number variants (CNVs) have been linked to neurodevelopmental disorders such as inte...