2021 (v1)
Publication
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Uploaded on: April 14, 2023
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2016 (v1)Publication
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Uploaded on: April 14, 2023 -
2021 (v1)Publication
Mutations in the PRRT2 gene are the main cause for a group of paroxysmal neurological diseases including paroxysmal kinesigenic dyskinesia, episodic ataxia, benign familial infantile seizures, and hemiplegic migraine. In the mature central nervous system, the protein has both a functional and a structural role at the synapse. Indeed, PRRT2...
Uploaded on: October 11, 2023