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pro vyhledávání: '"L. Van Casteren, MD."'
Autor:
T. Robyns, MD., D. Nuyens, MD., PhD., L. Van Casteren, MD., A. Corveleyn, PhD., T. De Ravel, MD., PhD., H. Heidbuchel, MD., PhD., R. Willems, MD., PhD.
Publikováno v:
Indian Pacing and Electrophysiology Journal, Vol 14, Iss 3, Pp 133-149 (2014)
Mutations in the SCN5A gene are responsible for multiple phenotypical presentations including Brugada syndrome, long QT syndrome, progressive familial heart block, sick sinus syndrome, dilated cardiomyopathy, lone atrial fibrillation and multiple ove
Externí odkaz:
https://doaj.org/article/06ce1dd08f204abab9dac9ca7ba82c5d