Associated Papers
Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene.
Pater JA et al.
Human Genetics, 2022
35278131 (PubMed )
Supplement: 439_2022_2444_MOESM1_ESM.pdf
Select a paper to view details