Erratum: Sodium channel gene (SCN5A) mutations in 44 index patients with brugada syndrome: Different incidences in familial and sporadic disease |
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| Authors: | Eric Schulze‐Bahr Lars Eckardt Günter Breithardt Karlheinz Seidl Thomas Wichter Christian Wolpert Martin Borggrefe Wilhelm Haverkamp |
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| Affiliation: | 1. Department of Cardiology and Angiology, Hospital of the University of Münster, Münster, Germany;2. Group “Genetics of Arrhythmias,” Institute for Arteriosclerosis Research at the University of Münster, Münster, GermanyInstitut für Arterioskleroseforschung an der Universit?t Münster, Molekular‐Kardiologie, Domagkstr. 3, D‐48149 Münster, Germany;3. Group “Genetics of Arrhythmias,” Institute for Arteriosclerosis Research at the University of Münster, Münster, Germany;4. Department of Cardiology of the Klinikum der Stadt Ludwigshafen am Rhein, Ludwigshafen am Rhein, Germany;5. Department of Cardiology and Angiology, Hospital of the University of Mannheim, Mannheim, Germany |
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| Abstract: | In supplementation of previously published cardiac sodium channel (SCN5A) gene mutations that were cited in the text, in Table 2 and in Figure 2 we here apply an updated gene mutation nomenclature (Human Genome Variation Society, 2005) to facilitate mutation annotation comparison (SCN5A cDNA reference: NM_198056.1 or GI: 37622906; amino acid reference sequence: SWISS‐PROT entry Q14524, long splice variant, 2,016 amino acids): Mutation: c.2602delC Amino acid change: p.Glu868X Mutation: c.2581_2582delTT Amino acid change: p.Phe861Trp fsX90 Mutation: c.4477_4479delAAG Amino acid change: p.Lys1493del Mutation: c.5425C>A Amino acid change: p.Ser1812X |
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