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A common PRRT2 mutation in familial paroxysmal kinesigenic dyskinesia in Hong Kong: a case series of 16 patients
A common PRRT2 mutation in familial paroxysmal kinesigenic dyskinesia in Hong Kong: a case series of 16 patients
2016
Cy Law
Wl Yeung
Yf Cheung
Hf Chan
Eva Lw Fung
Joannie Hui
Iris Ok Yung
Yp Yuen
Angel Ok Chan
Christopher W.K. Lam
Keywords:
Surgery
Medicine
PRRT2
Pediatrics
Familial Paroxysmal Kinesigenic Dyskinesia
Mutation
Chorea
Correction
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