KCNJ2 mutations in arrhythmia patients referred for LQT testing: a mutation T305A with novel effect on rectification properties. [electronic resource]
Producer: 20070807Description: 323-9 p. digitalISSN:- 1547-5271
- Adolescent
- Adult
- Aged
- Arrhythmias, Cardiac -- genetics
- Child
- Child, Preschool
- Electrophysiologic Techniques, Cardiac
- Female
- Gene Expression
- Genetic Predisposition to Disease
- Genetic Testing
- Genotype
- Humans
- Incidence
- Infant
- Infant, Newborn
- Long QT Syndrome -- genetics
- Male
- Middle Aged
- Mutation, Missense
- Phenotype
- Potassium Channels, Inwardly Rectifying
- Ryanodine Receptor Calcium Release Channel -- genetics
- Tachycardia, Ventricular -- genetics
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Publication Type: Journal Article; Research Support, N.I.H., Extramural
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