Identification of three novelTECTA mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locus

  • Nicole C. Meyer, Fatemeh Alasti, Carla J. Nishimura, Parisa Imanirad, Kimia Kahrizi, Yasser Riazalhosseini, Mahdi Malekpour, Nafiseh Kochakian, Payman Jamali, Guy Van Camp, Richard J.H. Smith, Hossein Najmabadi
  • American Journal of Medical Genetics Part A, July 2007, Wiley
  • DOI: 10.1002/ajmg.a.31718

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