Mutation detection in long QT syndrome: A comprehensive set of primers and PCR conditions [5]

Journal of Medical Genetics

Volumn 38, Issue 10, 2001, Pages 705-710

  Syrris, P ^a   Murray, A ^a   Carter, N D ^a   McKenna, W M ^a   Jeffery, S ^a  

^a ST GEORGE'S UNIVERSITY OF LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; POTASSIUM CHANNEL; PRIMER DNA; PROTEIN HERG; PROTEIN KCNQ1; PROTEIN SCN5A; SODIUM CHANNEL; UNCLASSIFIED DRUG;

EXON; GENE AMPLIFICATION; GENE MUTATION; GENE SEQUENCE; GENETIC CODE; GENETIC POLYMORPHISM; GENETIC RISK; HEART ARRHYTHMIA; LETTER; LONG QT SYNDROME; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; QT INTERVAL; SEQUENCE ANALYSIS; SUDDEN DEATH;

CATION TRANSPORT PROTEINS; DNA MUTATIONAL ANALYSIS; DNA PRIMERS; DNA-BINDING PROTEINS; ETHER-A-GO-GO POTASSIUM CHANNELS; EXONS; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; HUMANS; KCNQ POTASSIUM CHANNELS; KCNQ1 POTASSIUM CHANNEL; LONG QT SYNDROME; MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; POTASSIUM CHANNELS; POTASSIUM CHANNELS, VOLTAGE-GATED; REPRODUCIBILITY OF RESULTS; SENSITIVITY AND SPECIFICITY; SODIUM CHANNELS; TEMPERATURE; TRANS-ACTIVATORS;

EID: 0034796020     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

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