KCNT1

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Potassium channel subfamily T, member 1, also known as KCNT1 is a human gene that encodes the KCa4.1 protein. KCa4.1 is a member of the calcium-activated potassium channel protein family [1]

Associated Conditions

Mutations in the KCNT1 gene has been shown to be a cause of Early Infantile Epileptic Encephalopathy. [2]

See also

References

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Further reading

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