KCNT1
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
Associated Conditions
Mutations in the KCNT1 gene has been shown to be a cause of Early Infantile Epileptic Encephalopathy.
See also
References
Further reading
This page contains text from Wikipedia, the Free Encyclopedia - https://wn.com/KCNT1
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