IndraLab

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KCN activates KCNQ2. 3 / 3
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"A significant proportion of cases have a genetic origin, and the most frequently mutated gene is KCNQ2, encoding Kv7.2, a voltage dependent potassium channel subunit, leading to so called KCNQ2 related epileptic encephalopathy (KCNQ2-REE)."
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"In 1998, geneticists discovered that BFNC is caused by mutations in a novel potassium channel subunit, KCNQ2."
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"Potassium channel, voltage-gated, kqt-like subfamily, member 2 (KCNQ2) pathogenic variants cause benign neonatal epilepsy and KCNQ2-related encephalopathy."
| PMC