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Novel OTOA mutations cause autosomal recessive non‐syndromic hearing impairment in Pakistani families
Author(s) -
Lee K,
Chiu I,
SantosCortez RLP,
Basit S,
Khan S,
Azeem Z,
Andrade PB,
Kim SS,
Ahmad W,
Leal SM
Publication year - 2013
Publication title -
clinical genetics
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/cge.12047
Subject(s) - genetics , hearing loss , mutation , biology , medicine , gene , audiology
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