Genetic markers in the differential diagnosis in a family setting of episodic loss of consciousness by Thomas, Saralene Iona

Other Authors: “…Corfield, Valerie…”
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An investigation of myosin binding protein C mutations in South Africa and a search for ligands binding to myosin binding protein C by De Lange, W. J. (Willem Jacobus)

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A candidate and novel gene search to identify the PFHBII-causative gene by Fernandez, Pedro (Pedro Wallace)

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Bioinformatics-based strategies to identify PFHBII-causing and HCM main locus and/or HCM modifying mutations by Yako, Yandiswa

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Identifying ligands of the C-terminal domain of cardiac expressed connexin 40 and assessing its involvement in cardiac conduction disease by Keyser, Rowena J.

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Identification of the modulators of cardiac ion channel function by Carstens, Johanna J.

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Investigations of Renin-Angiotensin Aldosterone System (RAAS) genes in hypertrophy in hypertrophic cardiomyopathy (HCM) founder families by Cloete, Ruben Earl Ashley

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A candidate and novel gene search to identify the PFHBII-causative gene by Fernandez, Pedro

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Identification of novel CA repeat markers for use in fine mapping of the PFHBI gene and screening of the HRC candidate gene by Christoffels, Alan Gilbert

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Molecular and functional characterisation of Long QT Syndrome causing genes by Hedley, Paula Louise

Other Authors: “…Corfield, Valerie A.…”
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