Novel loss-of-function PRRT2mutation causes paroxysmal kinesigenic dyskinesia in a Han Chinese family
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,General Medicine
Link
http://link.springer.com/content/pdf/10.1186/1471-2377-14-146.pdf
Reference14 articles.
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2. Groffen AJ, Klapwijk T, van Rootselaar AF, Groen JL, Tijssen MA: Genetic and phenotypic heterogeneity in sporadic and familial forms of paroxysmal dyskinesia. J Neurol. 2013, 260: 93-99.
3. Sun W, Li J, Zhu Y, Yan X, Wang W: Clinical features of paroxysmal kinesigenic dyskinesia: report of 24 cases. Epilepsy Behav. 2012, 25: 695-699.
4. Bhaita KP: Paroxysmal dyskinesia. Mov Disord. 2011, 26: 1157-1165.
5. Bruno MK, Hallett M, Gwinn-Hardy K, Sorensen B, Considine E, Tucker S, Lynch DR, Mathews KD, Swoboda KJ, Harris J, Soong BW, Ashizawa T, Jankovic J, Renner D, Fu YH, Ptacek LJ: Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteria. Neurology. 2004, 63: 2280-2287.
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