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Human KCNQ5 de novo mutations underlie epilepsy and intellectual disability.
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Human KCNQ5 de novo mutations underlie epilepsy and intellectual disability.
Human KCNQ5 de novo mutations underlie epilepsy and intellectual disability. J Neurophysiol. 2022 07 01; 128(1):40-61.
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PubMed
subject areas
Animals
Child
Cricetinae
Cricetulus
Epilepsy
HEK293 Cells
Humans
Intellectual Disability
KCNQ Potassium Channels
Mice
Mutation, Missense
Seizures
authors with profiles
Jan-Marino Ramirez
William B. Dobyns