A novel variant of the SOX10 gene associated with Waardenburg syndrome type IV

Waardenburg syndrome (WS) is a rare genetic disorder characterized by varying degrees of sensorineural hearing loss and accumulated pigmentation in the skin, hair and iris. The syndrome is classified into four...

Source: BMC Medical Genomics - June 26, 2023 Category: Genetics & Stem Cells Authors: Yanan Wang, Yuqiong Chai, Pai Zhang and Weiwei Zang Tags: Case Report Source Type: research