De novo variants in GREB1L are associated with non-syndromic inner ear malformations and deafness

Here’s a research article about dnon-syndromic inner ear malformations and deafness that was written by Isabelle Schrauwen, Elina Kari, Jacob Mattox, Lorida Llaci, Joanna Smeeton, Marcus Naymik, David W. Raible, James A. Knowles, J. Gage Crump, Matthew J. Huentelman, Rick A. Friedman.