Novel OTOA mutations cause autosomal recessive non-syndromic hearing impairment in Pakistani families

K. Lee, I. Chiu, Rlp Santos-Cortez, S. Basit, S. Khan, Z. Azeem, Pb Andrade, Ss Kim, W. Ahmad, Sm Leal

Research output: Contribution to journalLetterpeer-review

10 Scopus citations
Original languageEnglish (US)
Pages (from-to)294-296
Number of pages3
JournalClinical Genetics
Issue number3
StatePublished - Sep 2013

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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