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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Bibliographic Details
Main Author: Waheed Ullah, Qazi
Format: Thesis (University of Nottingham only)
Language:English
Published: 2024
Subjects:
Online Access:https://eprints.nottingham.ac.uk/77313/

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