Novel mutations in the KCND3-encoded Kv4.3 K+ channel associated with autopsy-negative sudden unexplained death

Heritable arrhythmia syndromes, including Brugada syndrome (BrS) and idiopathic ventricular fibrillation (IVF), may serve as the pathogenic basis for autopsy‐negative sudden unexplained death (SUD) and sudden infant death syndrome (SIDS). Emerging evidence has linked perturbations in the transient o...

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Veröffentlicht in:	Human mutation 2012-06, Vol.33 (6), p.989-997
Hauptverfasser:	Giudicessi, John R., Ye, Dan, Kritzberger, Chad J., Nesterenko, Vladislav V., Tester, David J., Antzelevitch, Charles, Ackerman, Michael J.
Format:	Artikel
Sprache:	eng
Schlagworte:	Action Potentials Adolescent Adult Aged Amino Acid Sequence Amino Acid Substitution arrhythmia Autopsy Cell Line Child Child, Preschool Cohort Studies Death, Sudden, Cardiac - epidemiology Death, Sudden, Cardiac - etiology Female Humans Infant ion channels KCND3 Male Middle Aged Mutation pediatrics Prevalence Shal Potassium Channels - genetics Shal Potassium Channels - metabolism sudden death Sudden Infant Death - diagnosis Sudden Infant Death - epidemiology Sudden Infant Death - genetics Young Adult
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