Keyphrases
Splicing mutation
100%
Donor Splice Site
100%
Long QT Syndrome
100%
Mutation Type
66%
Affected Family Members
66%
Polymorphism Analysis
66%
Single-strand Conformation Polymorphism
66%
Amino Acid Variation
66%
DNA Sequencing
66%
Potassium
66%
Sodium
66%
Site Characteristics
33%
Kindred
33%
3' End
33%
KCNE1
33%
Polymerase Chain Reaction
33%
Outward Current
33%
Mutant Alleles
33%
New mutation
33%
Exon 6
33%
Repolarization
33%
Ion Channels
33%
Gene Coding
33%
Heart Cell
33%
SCN5A
33%
Cellular Machinery
33%
Splice Site
33%
Codon
33%
HERG
33%
Transmembrane Segment
33%
Normal Variants
33%
Point mutation
33%
Clinical Course
33%
K Channels
33%
Whole Blood
33%
Syncope
33%
Stop Codon
33%
DNA Fragments
33%
Biochemistry, Genetics and Molecular Biology
Splice Site Mutation
100%
Long QT Syndrome
100%
Conformation
66%
DNA Sequence
66%
Amino Acid
66%
Human Ether A Go Go Related Gene
33%
Exon
33%
Polymerase Chain Reaction
33%
Potassium Channel
33%
Point Mutation
33%
Ion Channel
33%
KCNE1
33%
Stop Codon
33%
Repolarization
33%
Codon
33%
Allele
33%
Immunology and Microbiology
Conformation
100%
DNA Sequence
100%
Amino Acid
100%
Polymerase Chain Reaction
50%
Repolarization
50%
Point Mutation
50%
Codon
50%
Exon
50%
Allele
50%
Potassium Channels
50%
Stop Codon
50%