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Erratum: Sodium channel gene (SCN5A) mutations in 44 index patients with brugada syndrome: Different incidences in familial and sporadic disease

✍ Scribed by Eric Schulze-Bahr; Lars Eckardt; Günter Breithardt; Karlheinz Seidl; Thomas Wichter; Christian Wolpert; Martin Borggrefe; Wilhelm Haverkamp

Publisher: John Wiley and Sons
Year: 2005
Tongue: English
Weight: 19 KB
Volume: 26
Category: Article
ISSN: 1059-7794
DOI: 10.1002/humu.9351

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✦ Synopsis

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.

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Sodium channel gene (SCN5A) mutations in 44 index patients with Brugada syndrome: Different incidences in familial and sporadic disease

✍ Eric Schulze-Bahr; Lars Eckardt; Günter Breithardt; Karlheinz Seidl; Thomas Wich 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 120 KB

The Brugada syndrome (BS) is a distinct form of idiopathic ventricular fibrillation and may cause sudden cardiac death in healthy young individuals. In the surface ECG, BS can be recognized by an atypical right bundle branch block and ST-segment elevation in the right precordial leads. Mutations in