Asystole in alternating hemiplegia with de novo ATP1A3 mutation

European Journal of Medical Genetics

Volumn 57, Issue 1, 2014, Pages 37-39

  Novy, Jan ^a,b   McWilliams, Eric ^c   Sisodiya, Sanjay M ^a,b  

^a UNIVERSITY COLLEGE LONDON HOSPITALS   (United Kingdom)

^b EPILEPSY SOCIETY   (United Kingdom)

^c St Leonards on Sea   (United Kingdom)

Author keywords

Arrhythmia; Mortality; Rapid onset dystonia parkinsonism; Seizures

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); SODIUM POTASSIUM ADENOSINE TRIPHOSPHATASE ALPHA3; UNCLASSIFIED DRUG;

ARTICLE; CONSCIOUSNESS DISORDER; DUAL CHAMBER PACEMAKER; ELECTROENCEPHALOGRAM; FOLLOW UP; HEART ARREST; HEMIPLEGIA; NUCLEAR MAGNETIC RESONANCE IMAGING; SEIZURE; TACHYCARDIA; TELEMETRY;

ARRHYTHMIA; MORTALITY; RAPID ONSET DYSTONIA-PARKINSONISM; SEIZURES;

DNA MUTATIONAL ANALYSIS; FEMALE; HEART ARREST; HEMIPLEGIA; HUMANS; MUTATION, MISSENSE; SODIUM-POTASSIUM-EXCHANGING ATPASE; YOUNG ADULT;

EID: 84892550770     PISSN: 17697212     EISSN: 18780849     Source Type: Journal    
DOI: 10.1016/j.ejmg.2013.11.003     Document Type: Article

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