PRRT2 mutation causes paroxysmal kinesigenic dyskinesia and hemiplegic migraine in monozygotic twins

European Journal of Paediatric Neurology

Volumn 17, Issue 3, 2013, Pages 254-258

  Castiglioni, Claudia ^a   López, Isabel ^a   Riant, Florence ^b   Bertini, Enrico ^c   Terracciano, Alessandra ^c  

^a CLÍNICA LAS CONDES   (Chile)

^b HÔPITAL LARIBOISIÈRE   (France)

^c BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

Author keywords

Hemiplegic migraine; Movement disorders; Neurogenetics; Paroxysmal kinesigenic dyskinesia

Indexed keywords

CARBAMAZEPINE; CLONAZEPAM; GENOMIC DNA; HALOPERIDOL; MEMBRANE PROTEIN; PROLINE RICH TRANSMEMBRANE PROTEIN 2; UNCLASSIFIED DRUG;

ADULT; ARTICLE; CASE REPORT; CONVULSION; DYSKINESIA; FEBRILE CONVULSION; GENE MUTATION; GENETIC ANALYSIS; HEMIPLEGIC MIGRAINE; HUMAN; MAGNETIC RESONANCE ANGIOGRAPHY; MALE; MONOZYGOTIC TWINS; PAROXYSMAL KINESIGENIC DYSKINESIA; PRIORITY JOURNAL;

ADULT; CHOREA; COMORBIDITY; DISEASES IN TWINS; GENOTYPE; HUMANS; MALE; MEMBRANE PROTEINS; MIGRAINE DISORDERS; MUTATION; NERVE TISSUE PROTEINS; PEDIGREE; TWINS, MONOZYGOTIC; YOUNG ADULT;

EID: 84875846094     PISSN: 10903798     EISSN: 15322130     Source Type: Journal    
DOI: 10.1016/j.ejpn.2012.10.010     Document Type: Article

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