Author: Corfield, Valerie A.
Similar Items: Molecular and functional characterisation of Long QT Syndrome causing genes
- An investigation of the clinical profile and extent of Long QT Syndrome (LQTS) associated with the KCNQ1-A341V mutation in South Africa and with the KCNH2-A1116V mutation in an Italian family and the role that autonomic nervous system (ANS) activity and genetics play in clinical variability
- Long QT syndrome : the identification and verification of putative KCNE2-interacting proteins
- Identification of the modulators of cardiac ion channel function
- The search for tourette syndrome genes : a conceptual and experimental approach
- Analysis of the potassium voltage-gated channel subfamily Q member 1 gene in sudden unexplained deaths in a South African population
- Electrocardiographic predictors of poor outcome in acute myocardial infarction