Molecular Mechanisms of Epileptic Encephalopathy Caused by KCNMA1 Loss-of-Function Mutations
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DOI: 10.3389/fphar.2021.775328
Abstract: The gene kcnma1 encodes the α-subunit of high-conductance calcium- and voltage-dependent K+ (BK) potassium channel. With the development of generation gene sequencing technology, many KCNMA1 mutants have been identified and are more closely related to… read more here.
Keywords: mechanisms epileptic; loss function; molecular mechanisms; loss ... See more keywords