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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, SMVolume:
84
Language:
english
Journal:
Clinical Genetics
DOI:
10.1111/cge.12047
Date:
September, 2013
File:
PDF, 551 KB
english, 2013