Clinical heterogeneity of the SLC26A4 gene in UAE patients with hearing loss and bioinformatics investigation of DFNB4/Pendred syndrome missense mutations

xlomafota13 shared this article with you from Inoreader Clinical heterogeneity of the <em>SLC26A4</em> gene in UAE patients with hearing loss and bioinformatics investigation of DFNB4/Pendred syndrome missense mutations Via International Journal of Pediatric Otorhinolaryngology Publication date: Available online 9 November 2020 Source: International Journal of Pediatric Otorhinolaryngology Author(s): Jihen Chouchen, Mona Mahfood, Maryam Alobathani, Walaa Kamal Eldin Mohamed, Abdelaziz Tlili View on the web Inoreader. Take back control of your news feed. Follow us on Twitter and Facebook.