R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation. [electronic resource]
Producer: 20110524Description: 48-55 p. digitalISSN:- 1556-3871
- Adult
- Atrial Fibrillation -- genetics
- Computational Biology
- Female
- Genetic Pleiotropy -- genetics
- Genetic Predisposition to Disease -- genetics
- Humans
- KCNQ1 Potassium Channel -- genetics
- Male
- Mutation, Missense
- Patch-Clamp Techniques
- Pedigree
- Phenotype
- Polymorphism, Single Nucleotide
- Romano-Ward Syndrome -- genetics
No physical items for this record
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.