Alpha-1 Antitrypsin Deficiency.
Methods in molecular biology (Clifton, N.J.), 2750: 1-7 PMID 38108962 DOI 10.1007/978-1-0716-3605-3_1
Abstract
Alpha-1 antitrypsin (AAT) deficiency is a common monogenic disorder in which there is a strong founder effect of a single missense mutation in SERPINA1, the gene encoding this major circulating serum anti-protease that is normally expressed primarily in hepatocytes. These features make AAT deficiency particularly attractive as a target for therapeutic gene editing using a wide variety of approaches.