QuickView for ATP11A;jsessionid=C8FE9F387FC417A5C58603272FF1714A (gene)

1. A mutation in ATP11A causes autosomal-dominant auditory neuropathy type 2.
2. ATP11A promotes EMT by regulating Numb PRRL in pancreatic cancer cells.
3. Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice a…
4. Disease Mutation Study Identifies Critical Residues for Phosphatidylserine Flippase ATP11A.
5. DNA Methylation at ATP11A cg11702988 Is a Biomarker of Lung Disease Severity in Cystic Fibrosis: A L…

There were no clinical trials for ATP11A;jsessionid=C8FE9F387FC417A5C58603272FF1714A