
Alpha-1 antitrypsin deficiency (AATD), linked to SERPINA1 gene mutations, often goes undiagnosed, leading to severe conditions like pulmonary emphysema and liver disease. Beyond common variants like S (E264V) and Z (E342K), this study reveals 20 new SERPINA1 mutations, including 4 null and 16 missense alleles. The results identified two severe deficiency mutants (Smilano and Mcampolongo) and three milder variants (Xsarezzo, Pdublin, and Ctiberias). This multidisciplinary approach underscores the importance of bioinformatics tools like REVEL in assessing rare AAT variants, aiding diagnosis and care.
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