Keyphrases
Epilepsy
100%
Loss Function
100%
Dyskinesia
100%
Biallelic
100%
Allelic Loss
100%
CACNA1B
100%
CaV2.2
50%
Synaptic
25%
Motor Control
25%
Pore-forming Subunit
25%
Normal Human
25%
Causative mutation
25%
Neurotransmission
25%
Seizure
25%
Pathogenic Mechanism
25%
Gain-of-function mutation
25%
Neuronal Function
25%
Epileptic Encephalopathy
25%
Synaptic Activity
25%
Infantile Epileptic Encephalopathy
25%
Ca2+ Influx
25%
Developmental Delay
25%
All-affected
25%
Involuntary Movement
25%
Soluble N-ethylmaleimide-sensitive Factor Attachment Protein Receptor (SNARE)
25%
Hypotonia
25%
Early Postnatal Period
25%
Respiratory Complications
25%
Neurological Features
25%
Voltage-gated Calcium Channels
25%
Hyperkinetic Movements
25%
Mean Age of Death
25%
Nonepileptic
25%
Neurological Syndrome
25%
Hyperkinetic Movement Disorders
25%
Postnatal Microcephaly
25%
Human Neurodevelopment
25%
Neuroscience
Dyskinesia
100%
Synaptic Transmission
100%
Brain Disease
100%
Hypotonia
50%
Microcephaly
50%
Motor Control
50%
Nerve Cell Differentiation
50%
Voltage Gated Calcium Channel
50%
Stereotypic Movement Disorder
50%
Biochemistry, Genetics and Molecular Biology
Synaptic Transmission
100%
Nerve Cell Differentiation
50%
Motor Control
50%
Normal Human
50%
Involuntary Movement
50%
Perinatal Period
50%
Voltage Gated Calcium Channel
50%