Novel Mutations in the KCND3-Encoded Kv4.3 K+ Channel Associated with Autopsy-Negative Sudden Unexplained Death

Human Mutation

Volumn 33, Issue 6, 2012, Pages 989-997

  Giudicessi, John R ^a,b,c   Ye, Dan ^a,b   Kritzberger, Chad J ^c   Nesterenko, Vladislav V ^d   Tester, David J ^a,b   Antzelevitch, Charles ^d   Ackerman, Michael J ^a,b  

^a MAYO CLINIC   (United States)

^b MAYO GRADUATE SCHOOL   (United States)

^c MAYO CLINIC COLLEGE OF MEDICINE   (United States)

^d MASONIC MEDICAL RESEARCH LABORATORY   (United States)

Author keywords

Arrhythmia; Ion channels; Kcnd3; Pediatrics; Sudden death

Indexed keywords

POTASSIUM CHANNEL; POTASSIUM CHANNEL KV4.3; UNCLASSIFIED DRUG; VALINE;

ADULT; AGED; ALLELE; ARTICLE; AUTOPSY; BRUGADA SYNDROME; DENATURATION; ELECTROPHYSIOLOGY; FEMALE; GENE MUTATION; GENETIC VARIABILITY; HEART ARRHYTHMIA; HEART VENTRICLE FIBRILLATION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; HUMAN CELL; MALE; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SUDDEN DEATH; SUDDEN INFANT DEATH SYNDROME; WILD TYPE;

ACTION POTENTIALS; ADOLESCENT; ADULT; AGED; AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; AUTOPSY; CELL LINE; CHILD; CHILD, PRESCHOOL; COHORT STUDIES; DEATH, SUDDEN, CARDIAC; FEMALE; HUMANS; INFANT; MALE; MIDDLE AGED; MUTATION; PREVALENCE; SHAL POTASSIUM CHANNELS; SUDDEN INFANT DEATH; YOUNG ADULT;

EID: 84865193189     PISSN: 10597794     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.22058     Document Type: Article

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