Article

Phenotypic variability and genetic characteristics of PRRT2-associated paroxysmal movement disorders in 13 Chinese families

2021-03-10

Abstract excerpt

<title>Abstract</title> <p><italic>PRRT2</italic>-associated paroxysmal movement disorders (<italic>PRRT2</italic>-PxMDs) include paroxysmal kinesigenic dyskinesias (PKD), benign familial infantile epilepsy (BFIE), infantile convulsions and choreoathetosis (ICCA), episodic ataxia (EA), paroxysmal nonkinesiasgenic dyskinesias (PNKD), and, in addition, other childhood-onset movement disorders and different types of...

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Literature Corpus work: a4c5e003-6125-55ba-ab54-57a65894b54b
DOI: 10.21203/rs.3.rs-288854/v1

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