Scientists have identified mutations in the CPD gene as a key cause of a rare congenital hearing loss, revealing how ...

Mutations in a gene known as CPD play a crucial role in a rare form of congenital hearing loss, an international team of ...

Researchers in Göttingen, Germany, have elucidated the structure and function of otoferlin, a protein that plays a crucial ...

In a small pivotal trial of an investigational gene therapy, most cases of congenital profound deafness from genetic variants ...

That’s where CEID comes in. It’s a preschool program that assesses each child and develops a personalized approach to ...

When she was born, doctors informed Opal Sandy’s parents that their child would never hear. At the age of 11 months, she had ...