Similar Items: Long QT syndrome : the identification and verification of putative KCNE2-interacting proteins
- 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
- Molecular and functional characterisation of Long QT Syndrome causing genes
- Identification of the modulators of cardiac ion channel function
- The search for tourette syndrome genes : a conceptual and experimental approach
- A molecular investigation of Waardenburg syndrome in Southern Africa
- Analysis of the potassium voltage-gated channel subfamily Q member 1 gene in sudden unexplained deaths in a South African population
Author: Kinnear, Craig
- Identification of variants responsible for primary immunodeficiency disease in South African patients using whole genome sequencing
- SNP discovery and selection in Cape buffalo for bTB association study, using an African buffalo genome reference
- Identification of novel candidate genes for susceptibility to tuberculosis by identifying disease-causing mutations in individuals with Primary Immunodeficiency disorders
- Identification of novel ligands of WDR47, using yeast two-hybrid analysis
- Tracking autophagy progression in mycobacterium tuberculosis-infected macrophages.
- Genome-Wide Associations Between Human Genotypes and Mycobacterium tuberculosis Clades Causing Disease