{"identifier":"nobleid:/w1/20260525/80638726","arkIdentifier":"ark:/48914/w1/20260525/80638726","version":1,"workTitle":"Mutation in second exon of MYO15A gene cause of nonsyndromic hearing loss and its association in the Arab population in Iran","workType":"Journal Article","authors":"Samira Asgharzade, Morteza Hashemzadeh Chaleshtori, Mohammad Tabatabaifar, Somayeh Reisi, M H Modaressi","description":null,"workUrl":null,"existingDoi":"10.2298/gensr1602587a","createdAt":"2026-05-25T15:20:49.944076Z","canonicalUrl":"https://nobleid.org/ark:/48914/w1/20260525/80638726.v1"}