Enhanced slow inactivation contributes to dysfunction of a recurrent SCN2A mutation associated with developmental and epileptic encephalopathy

Surobhi Ganguly, Christopher H. Thompson, Alfred L. George*

*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

9 Scopus citations

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Medicine and Dentistry

Biochemistry, Genetics and Molecular Biology

Neuroscience