Whole exome sequencing, in silico and functional studies confirm the association of the GJB2 mutation p.Cys169Tyr with deafness and suggest a role for the TMEM59 gene in the hearing process

Publication date: Available online 20 April 2021Source: Saudi Journal of Biological SciencesAuthor(s): Mona Mahfood, Jihen Chouchen, Walaa Kamal Eddine Ahmad Mohamed, Abdullah Al Mutery, Rania Harati, Abdelaziz Tlili
Source: Saudi Journal of Biological Sciences - Category: Biology Source Type: research