"We are not alone": ion channel mutations in a long QT syndrome cohort.

Anderson, Mark E

"We are not alone": ion channel mutations in a long QT syndrome cohort. [electronic resource] - Heart rhythm Oct 2005 - 1106-7 p. digital

Publication Type: Comment; Editorial; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.

1547-5271

10.1016/j.hrthm.2005.07.024 doi


Cohort Studies
Genetic Predisposition to Disease--genetics
Genetic Testing
Humans
Long QT Syndrome--diagnosis
Mutation, Missense--genetics
Polymorphism, Genetic--genetics
Ryanodine Receptor Calcium Release Channel--genetics
Tachycardia, Ventricular--genetics
Ventricular Fibrillation--genetics