Alpha-1 antitrypsin deficiency (AATD) is a genetic disorder characterized by the misfolding and accumulation of the mutant variant of alpha-1 antitrypsin (AAT) within hepatocytes, which limits its access to the circulation and exposes the lungs to protease-mediated tissue damage.
Bath Babylab to explore how young children see and interact with the world
A new facility at the University of Bath will officially open its doors this weekend (Saturday 24 June) at a public event to showcase the work of