Mutation Screening of KCNQ1 and KCNE1 Genes in Iranian Patients With Jervell and Lange-Nielsen Syndrome. [electronic resource]
Producer: 20200224Description: 273-281 p. digitalISSN:- 1551-3823
- DNA Mutational Analysis
- Family Health
- Female
- Frameshift Mutation
- Genetic Association Studies
- Heterozygote
- Homozygote
- Humans
- Iran -- epidemiology
- Jervell-Lange Nielsen Syndrome -- genetics
- KCNQ1 Potassium Channel -- genetics
- Male
- Pedigree
- Polymerase Chain Reaction
- Polymorphism, Single Nucleotide
- Potassium Channels, Voltage-Gated -- genetics
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Publication Type: Journal Article
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