Table B.

OMIM Entries for PRRT2-Associated Paroxysmal Movement Disorders (View All in OMIM)

128200EPISODIC KINESIGENIC DYSKINESIA 1; EKD1
602066CONVULSIONS, FAMILIAL INFANTILE, WITH PAROXYSMAL CHOREOATHETOSIS; ICCA
605751SEIZURES, BENIGN FAMILIAL INFANTILE, 2; BFIS2
611913CHROMOSOME 16p11.2 DELETION SYNDROME, 593-KB
614386PROLINE-RICH TRANSMEMBRANE PROTEIN 2; PRRT2

From: PRRT2-Associated Paroxysmal Movement Disorders

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