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High Risk for Bradyarrhythmic Complications in Patients With Brugada Syndrome Caused by SCN5A Gene Mutations

✍ Scribed by Takeru Makiyama; Masaharu Akao; Keiko Tsuji; Takahiro Doi; Seiko Ohno; Kotoe Takenaka; Atsushi Kobori; Tomonori Ninomiya; Hidetada Yoshida; Makoto Takano; Naomasa Makita; Fumiko Yanagisawa; Yukei Higashi; Youichi Takeyama; Toru Kita; Minoru Horie

Book ID
119265453
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
444 KB
Volume
46
Category
Article
ISSN
1558-3597

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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.