机译:Clinical and genetic analyses of 150 patients with paroxysmal kinesigenic dyskinesia
Shanghai Jiao Tong University,Shanghai Jiao Tong Univ;
Dept Neurol,Shanghai Jiao Tong Univ;
PRRT2; 16p11; 2 Microdeletion; Genotype-phenotype correlation; Paroxysmal kinesigenic dyskinesia; FAMILIAL INFANTILE EPILEPSY; PRRT2 MUTATIONS; CAUSATIVE GENE; IDENTIFICATION; CONVULSIONS; SEIZURES; 16P11.2; CHOREOATHETOSIS; MICRODELETION; ASSOCIATION;