A novel long-QT 5 gene mutation in the C-terminus (V109I) is associated with a mild phenotype. [electronic resource]
Producer: 20020114Description: 504-9 p. digitalISSN:- 0946-2716
- Alleles
- Animals
- Electrophysiology
- Female
- Heterozygote
- Humans
- Long QT Syndrome -- genetics
- Male
- Mutation
- Mutation, Missense
- Pedigree
- Phenotype
- Polymorphism, Single-Stranded Conformational
- Potassium Channels -- genetics
- Potassium Channels, Voltage-Gated
- RNA, Complementary -- metabolism
- Sequence Analysis, DNA
- Time Factors
- Xenopus
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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