Identical ATP1A3 mutation causes alternating hemiplegia of childhood and rapid-onset dystonia parkinsonism phenotypes

Pediatric Neurology

Volumn 51, Issue 6, 2014, Pages 850-853

  Boelman, Cyrus ^a   Lagman Bartolome, Ana Marissa ^a   MacGregor, Daune L ^a   McCabe, Jane ^a   Logan, Willam J ^a   Minassian, Berge A ^a  

^a HOSPITAL FOR SICK CHILDREN   (Canada)

Author keywords

Alternating hemiplegia of childhood; ATP1A3; Genetics; Movement disorder; Rapid onset dystonia parkinsonism; Topiramate

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); ATP1A3 PROTEIN; FLUNARIZINE; LORAZEPAM; SODIUM CHANNEL NAV1.1; TOPIRAMATE; UNCLASSIFIED DRUG;

ALTERNATING HEMIPLEGIA OF CHILDHOOD; ARTICLE; CASE REPORT; CHILD; EXON; GENE MUTATION; GENE SEQUENCE; HEMIPLEGIA; HUMAN; MISSENSE MUTATION; MONOTHERAPY; MOTOR DYSFUNCTION; PHENOTYPE; RAPID ONSET DYSTONIA PARKINSONISM;

EID: 84912083579     PISSN: 08878994     EISSN: 18735150     Source Type: Journal    
DOI: 10.1016/j.pediatrneurol.2014.08.015     Document Type: Article

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