Novel OTOA mutations cause autosomal recessive non-syndromic hearing impairment in Pakistani families.
Lee K; Chiu I; Santos-Cortez RL; Basit S; Khan S; Azeem Z; Andrade PB; Kim SS; Ahmad W; Leal SM; Clinical Genetics, 2013, vol. 84, issue 3, p 294, ISSN 13990004. ISBN 13990004.

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