RATIONALE:ABCA3 is a lipid transporter in the limiting membrane of lamellar bodies in alveolar type II cells. Mutations in the ABCA3 gene cause respiratory distress syndrome in new-borns and childhood interstitial lung disease. ABCA3 is N-terminally cleaved by an as yet unknown protease. a process believed to regulate ABCA3 activity. https://goodvibesbadhabiters.shop/product-category/masterseries/