KCNQ2
potassium voltage-gated channel subfamily Q member 2
Ассоциированные заболевания
Герминативная мутация (причина)6
Autosomal dominant non-syndromic intellectual disabilityORPHA:178469
→Self-limited neonatal epilepsyORPHA:1949
→Self-limited neonatal-infantile epilepsyORPHA:140927
→Self-limited infantile epilepsyORPHA:306
→Epilepsy of infancy with migrating focal seizuresORPHA:293181
→KCNQ2-related developmental and epileptic encephalopathyORPHA:439218
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