Paroxysmal disorders associated with PRRT2 mutations shake up expectations on ion channel genes

MeSH terms

• Ataxia / genetics*
• Chorea / genetics*
• Dyskinesias / diagnosis*
• Dyskinesias / genetics*
• Dystonia / genetics*
• Epilepsy, Benign Neonatal / diagnosis
• Epilepsy, Benign Neonatal / genetics*
• Female
• Genetic Linkage / genetics*
• Humans
• Male
• Membrane Proteins / genetics*
• Migraine Disorders / diagnosis*
• Migraine Disorders / genetics*
• Migraine with Aura / genetics*
• Mutation / genetics*
• Nerve Tissue Proteins / genetics*
• Phenotype*
• Seizures / diagnosis*
• Seizures / genetics*
• Seizures, Febrile / genetics*
• Spasms, Infantile / congenital*
• Spasms, Infantile / genetics