GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants

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作者： Koohiyan, Mahbobeh ^[1] ; Hashemzadeh-Chaleshtori, Morteza ^[2] ; Salehi, Mansoor ^[3] ; Abtahi, Hamidreza ^[4] ; Reiisi, Somayeh ^[5] ; Pourreza, Mohammad Reza ; Noori-Daloii, Mohammad Reza ; Tabatabaiefar, Mohammad Amin

作者单位： Univ Shahrekord, Fac Basic Sci, Dept Genet, Shahrekord, Iran ^[1] Isfahan Univ Med Sci, Sch Med, Dept Genet & Mol Biol, Hezarjarib St, Esfahan 817467346, Iran ^[2] Shahrekord Univ Med Sci, Basic Hlth Res Inst, Cellular & Mol Res Ctr, Shahrekord, Iran ^[3] Isfahan Univ Med Sci, Al Zahra Hosp, Dept Otolaryngol, Esfahan, Iran ^[4] Univ Tehran Med Sci, Sch Med, Dept Med Genet, Poursina Ave,16 Azar St,Keshavarz Blvd, Tehran ^[5]

关键词 Autosomal recessive non-syndromic hearing loss GJB2 c.35delG Iran

发布时间 2018-05-24

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International journal of pediatric otorhinolaryngology

2018年107卷

121-126页

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GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants

International journal of pediatric otorhinolaryngology

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International journal of pediatric otorhinolaryngology

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GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants

International journal of pediatric otorhinolaryngology

相似文献

International journal of pediatric otorhinolaryngology

相关期刊

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