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Journal Abstract Search

166 related items for PubMed ID: 28483220

  • 1. An update of common autosomal recessive non-syndromic hearing loss genes in Iranian population.
    Ghasemnejad T, Shekari Khaniani M, Zarei F, Farbodnia M, Mansoori Derakhshan S.
    Int J Pediatr Otorhinolaryngol; 2017 Jun; 97():113-126. PubMed ID: 28483220
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  • 3. Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review.
    Beheshtian M, Babanejad M, Azaiez H, Bazazzadegan N, Kolbe D, Sloan-Heggen C, Arzhangi S, Booth K, Mohseni M, Frees K, Azizi MH, Daneshi A, Farhadi M, Kahrizi K, Smith RJ, Najmabadi H.
    Arch Iran Med; 2016 Oct 01; 19(10):720-728. PubMed ID: 27743438
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  • 9. Identification of novel variants in Iranian consanguineous pedigrees with nonsyndromic hearing loss by next-generation sequencing.
    Bitarafan F, Seyedena SY, Mahmoudi M, Garshasbi M.
    J Clin Lab Anal; 2020 Dec 01; 34(12):e23544. PubMed ID: 32864763
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  • 11. Novel mutations in MYTH4-FERM domains of myosin 15 are associated with autosomal recessive nonsyndromic hearing loss.
    Mehregan H, Mohseni M, Jalalvand K, Arzhangi S, Nikzat N, Banihashemi S, Kahrizi K, Najmabadi H.
    Int J Pediatr Otorhinolaryngol; 2019 Feb 01; 117():115-126. PubMed ID: 30579064
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  • 12. Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a linked family.
    Reiisi S, Tabatabaiefar MA, Sanati MH, Chaleshtori MH.
    Iran J Basic Med Sci; 2016 Jul 01; 19(7):772-8. PubMed ID: 27635202
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  • 13. A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian family.
    Sarmadi A, Nasrniya S, Soleimani Farsani M, Narrei S, Nouri Z, Sepehrnejad M, Nilforoush MH, Abtahi H, Tabatabaiefar MA.
    BMC Med Genet; 2020 Jun 09; 21(1):127. PubMed ID: 32517708
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  • 15. Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees.
    Khatami S, Askari M, Bahreini F, Hashemzadeh-Chaleshtori M, Hematian S, Asgharzade S.
    BMC Med Genet; 2020 Nov 18; 21(1):226. PubMed ID: 33208113
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  • 18. Next generation sequencing and genetics of hereditary hearing loss in the iranian population: New insights from a systematic review.
    Koohiyan M.
    Int J Pediatr Otorhinolaryngol; 2020 Feb 18; 129():109756. PubMed ID: 31704577
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  • 20. The conserved p.Arg108 residue in S1PR2 (DFNB68) is fundamental for proper hearing: evidence from a consanguineous Iranian family.
    Hofrichter MAH, Mojarad M, Doll J, Grimm C, Eslahi A, Hosseini NS, Rajati M, Müller T, Dittrich M, Maroofian R, Haaf T, Vona B.
    BMC Med Genet; 2018 May 18; 19(1):81. PubMed ID: 29776397
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