Usher Syndrome Type 2 in An Iranian Family: A Novel Founder Variation in The USH2A Gene
Cell J. 2024 Aug 11;26(6):392-397. doi: 10.22074/cellj.2024.2024223.1521. ABSTRACT This study delves into Usher syndrome type 2 (USH2), an uncommon genetic disorder characterized by sensorineural hearing …