A common single nucleotide polymorphism can exacerbate long-QT type 2 syndrome leading to sudden infant death

Eyal Nof, Jonathan M Cordeiro, Guillermo J Pérez, Fabiana S Scornik, Kirstine Calloe, Barry Love, Elena Burashnikov, Gabriel Caceres, Moshe Gunsburg, Charles Antzelevitch

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

48 Citationer (Scopus)

Abstract

Udgivelsesdato: 2010-Apr
OriginalsprogEngelsk
TidsskriftCirculation. Cardiovascular genetics
Vol/bind3
Udgave nummer2
Sider (fra-til)199-206
Antal sider7
DOI
StatusUdgivet - 2010

Bibliografisk note

Keywords: Animals; CHO Cells; Codon, Nonsense; Cricetinae; Cricetulus; Death, Sudden, Cardiac; Electrophysiology; Ether-A-Go-Go Potassium Channels; Female; Genetic Counseling; Heterozygote; Humans; Infant; Long QT Syndrome; Pedigree; Polymorphism, Single Nucleotide; Pregnancy; Young Adult

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