Mutation detection in long QT syndrome: a comprehensive set of primers and PCR conditions

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Bibliographische Detailangaben
Veröffentlicht in:	Journal of medical genetics 2001-10, Vol.38 (10), p.705-710
Hauptverfasser:	Syrris, P, Murray, A, Carter, N D, McKenna, W M, Jeffery, S
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences Cation Transport Proteins Complex syndromes Diagnosis DNA Mutational Analysis - methods DNA Primers - genetics DNA-Binding Proteins ERG1 Potassium Channel Ether-A-Go-Go Potassium Channels Exons - genetics Gene mutations Genetic disorders Genetic Predisposition to Disease - genetics Genetic Testing - methods Humans KCNQ Potassium Channels KCNQ1 Potassium Channel Letters to the Editor Long QT Syndrome - genetics Medical genetics Medical sciences Mutation - genetics NAV1.5 Voltage-Gated Sodium Channel Polymerase chain reaction Polymerase Chain Reaction - methods Polymorphism, Single-Stranded Conformational Potassium Channels - genetics Potassium Channels, Voltage-Gated Reproducibility of Results Sensitivity and Specificity Sodium Channels - genetics Temperature Trans-Activators Transcriptional Regulator ERG
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