Mutation detection in congenital long QT syndrome: cardiac channel gene screen using PCR, dHPLC, and direct DNA sequencing. [electronic resource]
- Methods in molecular medicine 2006
- 181-207 p. digital
Publication Type: Journal Article
1543-1894
10.1385/1-59745-159-2:181 doi
Animals Base Sequence Chromatography, High Pressure Liquid--methods DNA Mutational Analysis--methods Humans Long QT Syndrome--genetics Mutation--genetics Polymerase Chain Reaction--methods Polymorphism, Single-Stranded Conformational