- Clinical Manifestations in Paroxysmal Kinesigenic Dyskinesia Patients with Proline-Rich Transmembrane Protein 2 Gene Mutation
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Youn J, Kim JS, Lee M, Lee J, Roh H, Ki CS, Choa JW
- KMID: 2400175
- J Clin Neurol.
- 2014 Jan;10(1):50-54.
BACKGROUND AND PURPOSE: Given the diverse phenotypes including combined non-dyskinetic symptoms in patients harboring mutations of the gene encoding proline-rich transmembrane protein 2 (PRRT2), the clinical significance of these mutations... -
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