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Novel sodium channel SCN5A mutations in Brugada syndrome patients from Greece

✍ Scribed by Christina-Maria Kotta; Aris Anastasakis; Konstantinos Gatzoulis; Antonis S. Manolis; Christodoulos Stefanadis

Book ID
116548169
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
238 KB
Volume
145
Category
Article
ISSN
0167-5273

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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

Erratum: Sodium channel gene (SCN5A) mut
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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.