Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

INIS

• losses 100%
• children 66%
• mutations 66%
• epilepsy 66%
• humans 33%
• control 33%
• death 33%
• voltage 33%
• motors 33%
• calcium 33%
• microcephaly 33%

Biochemistry, Genetics and Molecular Biology

• Mutation 66%
• Neurotransmission 66%
• Development 33%
• Normal Human 33%
• Age 33%
• Perinatal Period 33%
• Voltage Gated Calcium Channel 33%
• Adolescence 33%
• Nerve Cell Differentiation 33%
• Involuntary Movement 33%
• Introspection 33%
• Motor Control 33%
• Childhood 33%
• Movement (Physiology) 33%

Neuroscience

• Neurotransmission 66%
• Epilepsy 66%
• Encephalopathy 66%
• Nerve Cell Differentiation 33%
• Movement Disorder 33%
• Voltage Gated Calcium Channel 33%
• Hypotonia 33%
• Dyskinesia 33%
• Seizure 33%
• Microcephaly 33%