Elucidating the role of Cdk13 and Prkd1 in heart development and congenital heart disease
Congenital heart disease (CHD) is the most common congenital anomaly, with an overall incidence of approximately 1% in the United Kingdom. Genetic causes include chromosomal abnormalities, copy number variants, and point mutations. Recent studies have used whole exome sequencing (WES) in large CHD c...
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| Format: | Thesis (University of Nottingham only) |
| Language: | English |
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2024
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| Online Access: | https://eprints.nottingham.ac.uk/77313/ |