QuickView for ABCA3;jsessionid=638157C7EE05C8601359C0D7BB485060;jsessionid=90EEE12D432CEBE41F7469D920C99E4D (gene)

1. Human pluripotent stem cell modeling of alveolar type 2 cell dysfunction caused by ABCA3 mutations.
2. Similarities and differences of interstitial lung disease associated with pathogenic variants in SFT…
3. ABCA3 and LZTFL1 Polymorphisms and Risk of COVID-19 in the Czech Population.
4. ABCA3-related interstitial lung disease beyond infancy.
5. ABCA3 mutation-induced congenital pulmonary surfactant deficiency: A case report.

There were no clinical trials for ABCA3;jsessionid=638157C7EE05C8601359C0D7BB485060;jsessionid=90EEE12D432CEBE41F7469D920C99E4D