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 journalLetter

6 Scopus citations
Original languageEnglish (US)
Pages (from-to)294-296
Number of pages3
JournalClinical Genetics
Volume84
Issue number3
DOIs
StatePublished - Sep 2013

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Lee, K., Chiu, I., Santos-Cortez, R., Basit, S., Khan, S., Azeem, Z., Andrade, P., Kim, S., Ahmad, W., & Leal, S. (2013). Novel OTOA mutations cause autosomal recessive non-syndromic hearing impairment in Pakistani families. Clinical Genetics, 84(3), 294-296. https://doi.org/10.1111/cge.12047