Voltage-gated calcium channels have an important role in neurotransmission. Aberrations affecting genes encoding the alpha subunit of these channels have been associated with epilepsy and neuropsychiatric disorders such as autism or schizophrenia. Here we report three patients with a genomic aberration affecting the CACNA2D1 gene encoding the alpha 2 delta subunit of these voltage-gated calcium channels. All three patients present with epilepsy and intellectual disability pinpointing the CACNA2D1 gene as an interesting candidate gene for these clinical features. Besides these characteristics, patient 2 also presents with obesity with hyperinsulinism, which is very likely to be caused by deletion of the CD36 gene
This review summarises genetic studies in which calcium channel genes have been connected to the spe...
CACNA1C encodes the alpha-1-subunit of a voltage-dependent L-type calcium channel expressed in human...
© 2019 American Society of Human Genetics The occurrence of non-epileptic hyperkinetic movements in ...
Voltage-gated calcium channels have an important role in neurotransmission. Aberrations affecting ge...
Abstract Background Epilepsy is a neurological disorder characterized by the potential to induce sei...
Mutations in CACNA1A, which encodes the principal subunit of the P/Q calcium channel, underlie episo...
The molecular basis of idiopathic generalized epilepsy remains poorly understood. Absence epilepsy w...
Several inherited human neurological disorders can be caused by mutations in genes encoding Ca2+ cha...
: Autism Spectrum Disorder (ASD) is a highly heterogeneous neuropsychiatric disorder with a strong g...
Contribution to epileptic encephalopathy (EE) of mutations in CACNA2D2, encoding a2d-2 subunit of Vo...
Abstract Developmental and epileptic encephalopathies (DEEs) are a group of severe epilepsies that a...
Contribution to epileptic encephalopathy (EE) of mutations in CACNA2D2, encoding α2δ-2 subunit of Vo...
Developmental and epileptic encephalopathies (DEEs) are severe neurodevelopmental disorders often be...
International audiencePurpose:CACNA1C encodes the alpha-1-subunit of a voltage-dependent L-type calc...
Developmental and epileptic encephalopathies (DEEs) are severe neurodevelopmental disorders often be...
This review summarises genetic studies in which calcium channel genes have been connected to the spe...
CACNA1C encodes the alpha-1-subunit of a voltage-dependent L-type calcium channel expressed in human...
© 2019 American Society of Human Genetics The occurrence of non-epileptic hyperkinetic movements in ...
Voltage-gated calcium channels have an important role in neurotransmission. Aberrations affecting ge...
Abstract Background Epilepsy is a neurological disorder characterized by the potential to induce sei...
Mutations in CACNA1A, which encodes the principal subunit of the P/Q calcium channel, underlie episo...
The molecular basis of idiopathic generalized epilepsy remains poorly understood. Absence epilepsy w...
Several inherited human neurological disorders can be caused by mutations in genes encoding Ca2+ cha...
: Autism Spectrum Disorder (ASD) is a highly heterogeneous neuropsychiatric disorder with a strong g...
Contribution to epileptic encephalopathy (EE) of mutations in CACNA2D2, encoding a2d-2 subunit of Vo...
Abstract Developmental and epileptic encephalopathies (DEEs) are a group of severe epilepsies that a...
Contribution to epileptic encephalopathy (EE) of mutations in CACNA2D2, encoding α2δ-2 subunit of Vo...
Developmental and epileptic encephalopathies (DEEs) are severe neurodevelopmental disorders often be...
International audiencePurpose:CACNA1C encodes the alpha-1-subunit of a voltage-dependent L-type calc...
Developmental and epileptic encephalopathies (DEEs) are severe neurodevelopmental disorders often be...
This review summarises genetic studies in which calcium channel genes have been connected to the spe...
CACNA1C encodes the alpha-1-subunit of a voltage-dependent L-type calcium channel expressed in human...
© 2019 American Society of Human Genetics The occurrence of non-epileptic hyperkinetic movements in ...