Paroxysmal hypnogenic dyskinesia is associated with mutations in the PRRT2 gene

Neurology: Genetics

Volumn 2, Issue 2, 2016, Pages

  Liu, Xiao Rong ^a   Huang, Dan ^a   Wang, Jie ^a   Wang, Yi Fan ^a   Sun, Hui ^a   Tang, Bin ^a   Li, Wen ^a   Lai, Jin Xing ^a   He, Na ^a   Wu, Mei ^a   Su, Tao ^a   Meng, Heng ^a   Shi, Yi Wu ^a   Li, Bing Mei ^a   Tang, Bei Sha ^b   Liao, Wei Ping ^a  

^a GUANGZHOU MEDICAL UNIVERSITY   (China)

^b CENTRAL SOUTH UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM ACTIVATED POTASSIUM CHANNEL ALPHA SUBUNIT; CARBAMAZEPINE; CHOLINERGIC RECEPTOR; CHOLINERGIC RECEPTOR NICOTINIC ALPHA 2; CHOLINERGIC RECEPTOR NICOTINIC ALPHA 4; CHOLINERGIC RECEPTOR NICOTINIC BETA 2; GLUCOSE TRANSPORTER 1; LAMOTRIGINE; MEMBRANE PROTEIN; MYOFIBRILLOGENESIS REGULATOR 1; OXCARBAZEPINE; PHENYTOIN; POTASSIUM CHANNEL SUBFAMILY T MEMBER 1; PROLINE RICH REGION TRANSMEMBRANE PROTEIN 2; UNCLASSIFIED DRUG; VALPROIC ACID;

ADOLESCENT; ADULT; AMINO ACID SEQUENCE; ARTICLE; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DYSKINESIA; EEG ABNORMALITY; ELECTROENCEPHALOGRAM; EXON; FAMILY HISTORY; GENE MUTATION; GENETIC ASSOCIATION; HUMAN; MISSENSE MUTATION; MONOTHERAPY; NONREM SLEEP; PAROXYSMAL HYPNOGENIC DYSKINESIA; PAROXYSMAL KINESIGENIC DYSKINESIA; PRESCHOOL CHILD; PRIORITY JOURNAL; REMISSION; SCHOOL CHILD; SLEEP DEPRIVATION; STOP CODON; TEMPORAL LOBE; YOUNG ADULT;

EID: 84989211824     PISSN: None     EISSN: 23767839     Source Type: Journal    
DOI: 10.1212/NXG.0000000000000066     Document Type: Article

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