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Refining the genetic architecture of inherited cardiomyopathies through case-control analyses

Abstract:

Inherited cardiomyopathies comprise a clinically and genetically heterogeneous group of heart muscle disorders, which are a major cause of heart disease and cardiac morbidity. Genetic testing for these conditions has been available for over a decade, and the number of genes incorporated into clinical test panels has increased significantly in recent years. However, rather than an increase in genetic diagnoses, this has resulted in a higher proportion of inconclusive results.

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Division:
MSD
Role:
Author

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Supervisor
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Supervisor
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Funding agency for:
Thomson, K
Grant:
NIHR-HCS-D13-04-006
Type of award:
DPhil
Level of award:
Doctoral
Awarding institution:
University of Oxford
Language:
English
UUID:
uuid:fdc0e9f5-5680-4164-a3a0-ea4d59f3af24
Deposit date:
2019-03-01

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