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    Contextualizing Genetics for Regional Heart Failure Care

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    Author
    Iyngkaran, P; Thomas, MC; Johnson, R; French, J; Ilton, M; McDonald, P; Hare, DL; Fatkin, D
    Date
    2016-01-01
    Source Title
    Current Cardiology Reviews
    Publisher
    BENTHAM SCIENCE PUBL LTD
    University of Melbourne Author/s
    Hare, David
    Affiliation
    Medicine and Radiology
    Metadata
    Show full item record
    Document Type
    Journal Article
    Citations
    Iyngkaran, P., Thomas, M. C., Johnson, R., French, J., Ilton, M., McDonald, P., Hare, D. L. & Fatkin, D. (2016). Contextualizing Genetics for Regional Heart Failure Care. CURRENT CARDIOLOGY REVIEWS, 12 (3), pp.231-242. https://doi.org/10.2174/1573403X12666160606123103.
    Access Status
    Open Access
    URI
    http://hdl.handle.net/11343/260008
    DOI
    10.2174/1573403X12666160606123103
    Abstract
    Congestive heart failure (CHF) is a chronic and often devastating cardiovascular disorder with no cure. There has been much advancement in the last two decades that has seen improvements in morbidity and mortality. Clinicians have also noted variations in the responses to therapies. More detailed observations also point to clusters of diseases, phenotypic groupings, unusual severity and the rates at which CHF occurs. Medical genetics is playing an increasingly important role in answering some of these observations. This developing field in many respects provides more information than is currently clinically applicable. This includes making sense of the established single gene mutations or uncommon private mutations. In this thematic series which discusses the many factors that could be relevant for CHF care, once established treatments are available in the communities; this section addresses a contextual role for medical genetics.

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