Letter to the Editor

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

  1. K Lee1,
  2. I Chiu1,2,
  3. RLP Santos-Cortez1,
  4. S Basit3,
  5. S Khan3,
  6. Z Azeem4,
  7. PB Andrade1,
  8. SS Kim1,
  9. W Ahmad3,
  10. SM Leal1,*

Article first published online: 23 NOV 2012

DOI: 10.1111/cge.12047

Additional Information

How to Cite

Lee K, Chiu I, Santos-Cortez RLP, Basit S, Khan S, Azeem Z, Andrade PB, Kim SS, Ahmad W, Leal SM. Novel OTOA mutations cause autosomal recessive non-syndromic hearing impairment in Pakistani families.

Author Information

  1. 1

    Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA

  2. 2

    Bobby R. Alford Department of Otolaryngology-Head and Neck Surgery, Baylor College of Medicine, Houston, TX, USA

  3. 3

    Department of Biochemistry, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, Pakistan

  4. 4

    Department of Biochemistry, AJK medical College, Muzaffarabad, Azad Jammu and Kashmir, Pakistan

* Corresponding: Suzanne M. Leal
Department of Molecular and Human Genetics
Baylor College of Medicine
Houston, Texas, USA
Tel.: +1 713 7984011
Fax: +1 713 7984012
e-mail: sleal@bcm.edu

Publication History

  1. Article first published online: 23 NOV 2012

Funded by

  • Higher Education Commission
  • National Institutes of Health (NIH) – National Institute of Deafness and Communication Disorders. Grant Number: DC03594 and DC011651
  • NIH. Grant Number: N01-HG-65403

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View Full Article with Supporting Information (HTML) Get PDF (560K)