Novel OTOA mutations cause autosomal recessive non-syndromic hearing impairment in Pakistani families.
Lee, K; Chiu, I; Santos-Cortez, RLP; Basit, S; Khan, S; Azeem, Z; Andrade, PB; Kim, SS; Ahmad, W; Leal, SM; Clinical Genetics, 2013, vol. 84, issue 3, p 294, ISSN 00099163. ISBN 13990004.

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