1. Novel OTOA mutations cause autosomal recessive non‐syndromic hearing impairment in Pakistani families. (23rd November 2012) Authors: Lee, K; Chiu, I; Santos‐Cortez, RLP; Basit, S; Khan, S; Azeem, Z; Andrade, PB; Kim, SS; Ahmad, W; Leal, SM Journal: Clinical genetics Issue: Volume 84:Number 3(2013:Sep.) Page Start: 294 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗