A novel missense mutation in GIPC3 causes sensorineural hearing loss in an Iranian family revealed by targeted next-generation sequencing

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作者： Asgharzade, Samira ^[1] ; Tabatabaiefar, Mohammad Amin ^[2] ; Mohammadi-asl, Javad ^[3] ; Chaleshtori, Morteza Hashemzadeh

作者单位： AhvazJundishapurUniv Med Sci, Sch Med, Dept Med Genet, Ahwaz, Iran ^[1] Isfahan Univ Med Sci, Sch Med, Dept Genet & Mol Biol, Esfahan, Iran ^[2] Shahrekord Univ Med Sci, Basic Hlth Sci Inst, Cellular & Mol Res Ctr, Shahrekord, Iran ^[3]

关键词 Deafness gene panel Non-syndromichearing loss Targeted next-generationsequencing

发布时间 2018-07-10

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International journal of pediatric otorhinolaryngology

2018年108卷

8-11页

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A novel missense mutation in GIPC3 causes sensorineural hearing loss in an Iranian family revealed by targeted next-generation sequencing

International journal of pediatric otorhinolaryngology

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International journal of pediatric otorhinolaryngology

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A novel missense mutation in GIPC3 causes sensorineural hearing loss in an Iranian family revealed by targeted next-generation sequencing

International journal of pediatric otorhinolaryngology

相似文献

International journal of pediatric otorhinolaryngology

相关期刊

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