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Digenic inheritance in autosomal recessive non-syndromic hearing loss cases carrying GJB2 heterozygote mutations: assessment of GJB4, GJA1, and GJC3.
Kooshavar D, Tabatabaiefar MA, Farrokhi E, Abolhasani M, Noori-Daloii MR, Hashemzadeh-Chaleshtori M. Kooshavar D, et al. Among authors: farrokhi e. Int J Pediatr Otorhinolaryngol. 2013 Feb;77(2):189-93. doi: 10.1016/j.ijporl.2012.10.015. Epub 2012 Nov 8. Int J Pediatr Otorhinolaryngol. 2013. PMID: 23141803
Two novel SLC26A4 mutations in Iranian families with autosomal recessive hearing loss.
Yazdanpanahi N, Chaleshtori MH, Tabatabaiefar MA, Noormohammadi Z, Farrokhi E, Najmabadi H, Shahbazi S, Hosseinipour A. Yazdanpanahi N, et al. Among authors: farrokhi e. Int J Pediatr Otorhinolaryngol. 2012 Jun;76(6):845-50. doi: 10.1016/j.ijporl.2012.02.056. Epub 2012 Mar 23. Int J Pediatr Otorhinolaryngol. 2012. PMID: 22444735
High carrier frequency of the GJB2 mutation (35delG) in the north of Iran.
Chaleshtori MH, Farrokhi E, Shahrani M, Kheiri S, Dolati M, Rad LH, Pour-Jafari H, Samani KG, Chaleshtori KS, Crosby AH. Chaleshtori MH, et al. Among authors: farrokhi e. Int J Pediatr Otorhinolaryngol. 2007 Jun;71(6):863-7. doi: 10.1016/j.ijporl.2007.02.005. Epub 2007 Apr 10. Int J Pediatr Otorhinolaryngol. 2007. PMID: 17428550
51 results