Subject
Now showing items 1-3 of 3
-
Bioinformatics-based strategies to identify PFHBII-causing and HCM main locus and/or HCM modifying mutations
(Stellenbosch : University of Stellenbosch, 2004-12)ENGLISH ABSTRACT: Progressive familial heart block type II (PFHBII) is an inherited cardiac conduction disorder of unknown aetiology, which has been described in a South African family. The disorder was mapped to a 2.9 ... -
Mutation screening of candidate genes and the development of polymorphic markers residing on chromosome 19q13.3, the progressive familial heart block I gene search area
(Stellenbosch : Stellenbosch University, 2000-03)ENGLISH ABSTRACT: Progressive familial heart block type I (PFHBI) is a cardiac ventricular conduction disorder of unknown cause associated with risk of sudden death, which has been described in several South African ... -
Shared genetic risk factors of intracranial, abdominal, and thoracic aneurysms
(American Heart Association, 2016-07-14)Background: Intracranial aneurysms (IAs), abdominal aortic aneurysms (AAAs), and thoracic aortic aneurysms (TAAs) all have a familial predisposition. Given that aneurysm types are known to co‐occur, we hypothesized that ...
