Phenotypes and PRRT2 mutations in Chinese families with benign familial infantile epilepsy and infantile convulsions with paroxysmal choreoathetosis

[21] Monaco AP(2012)Mutations in PRRT2 result in paroxysmal dyskinesias with marked variability in clinical expression J Med Genet 49 79-82

[22] Demirkiran M(2012)PRRT2 mutations cause hemiplegic migraine Neurology 79 2122-2124

[23] Jankovic J(2013)PRRT2 is mutated in familial and non-familial benign infantile seizures Eur J Paediatr Neurol 17 77-81

[24] Chen WJ(2013)Genetic analysis of PRRT2 for benign infantile epilepsy, infantile convulsions with choreoathetosis syndrome, and benign convulsions with mild gastroenteritis Brain Dev 35 524-530

[25] Lin Y(2013)Genetic and phenotypic heterogeneity in sporadic and familial forms of paroxysmal dyskinesia J Neurol 260 93-99

[26] Xiong ZQ(2012)PRRT2 mutations in paroxysmal kinesigenic dyskinesia with infantile convulsions in a Taiwanese cohort PLoS One 7 e38543-742

[27] Wei W(2012)The PRRT2 mutation c.649dupC is the so far most frequent cause of benign familial infantile convulsions Seizure 21 740-436

[28] Ni W(2013)Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance Epilepsia 54 425-240

[29] Tan GH(2013)Novel PRRT2 mutations in paroxysmal dyskinesia patients with variant inheritance and phenotypes Genes Brain Behav 12 234-1244

[30] Guo SL(2013)PRRT2-related disorders: further PKD and ICCA cases and review of the literature J Neurol 260 1234-648

[21] Monaco AP(2012)Mutations in PRRT2 result in paroxysmal dyskinesias with marked variability in clinical expression J Med Genet 49 79-82

[22] Demirkiran M(2012)PRRT2 mutations cause hemiplegic migraine Neurology 79 2122-2124

[23] Jankovic J(2013)PRRT2 is mutated in familial and non-familial benign infantile seizures Eur J Paediatr Neurol 17 77-81

[24] Chen WJ(2013)Genetic analysis of PRRT2 for benign infantile epilepsy, infantile convulsions with choreoathetosis syndrome, and benign convulsions with mild gastroenteritis Brain Dev 35 524-530

[25] Lin Y(2013)Genetic and phenotypic heterogeneity in sporadic and familial forms of paroxysmal dyskinesia J Neurol 260 93-99

[26] Xiong ZQ(2012)PRRT2 mutations in paroxysmal kinesigenic dyskinesia with infantile convulsions in a Taiwanese cohort PLoS One 7 e38543-742

[27] Wei W(2012)The PRRT2 mutation c.649dupC is the so far most frequent cause of benign familial infantile convulsions Seizure 21 740-436

[28] Ni W(2013)Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance Epilepsia 54 425-240

[29] Tan GH(2013)Novel PRRT2 mutations in paroxysmal dyskinesia patients with variant inheritance and phenotypes Genes Brain Behav 12 234-1244

[30] Guo SL(2013)PRRT2-related disorders: further PKD and ICCA cases and review of the literature J Neurol 260 1234-648