"We are not alone": ion channel mutations in a long QT syndrome cohort. [electronic resource]
Producer: 20060213Description: 1106-7 p. digitalISSN:- 1547-5271
- 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
No physical items for this record
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.
There are no comments on this title.
Log in to your account to post a comment.