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발작성 운동 이상증 한국인 환자의 임상 및 유전자 분석

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Fig. 1.  Pedigrees of six paroxysmal kinesigenic dyskinesia (PKD) families. Pedigrees A, B, C, and D represent familial PKD, and pedigrees  D and E are for sporadic PKD
Table 1. Demographic Data and Clinical Features of 11 Clinically Diagnosed Paroxysmal Kinesigenic Dyskinesia (PKD) Patients
Table 3.  The Results of PRRT2 Gene Mutation Analysis of Korean Patients with PKD (including review of two literatures)

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