Clinical heterogeneity of the SLC26A4 gene in UAE patients with hearing loss and bioinformatics investigation of DFNB4/Pendred syndrome missense mutations.
International journal of pediatric otorhinolaryngology | 2021-01-01 | PMID 33199029
Chouchen Jihen, Mahfood Mona, Alobathani Maryam and 2 more
