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Novel pore mutation in SCN5A manifests as a spectrum of phenotypes ranging from atrial flutter, conduction disease, and Brugada syndrome to sudden cardiac death

✍ Scribed by Rossenbacker, Tom; Carroll, Sheila J.; Liu, Huajun; Kuipéri, Cuno; de Ravel, Thomy J.L.; Devriendt, Koen; Carmeliet, Peter; Kass, Robert S.; Heidbüchel, Hein


Book ID
123200704
Publisher
Elsevier Science
Year
2004
Tongue
English
Weight
213 KB
Volume
1
Category
Article
ISSN
1547-5271

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