Diverse pattern of gap junction beta-2 and gap junction beta-4 genes mutations and lack of contribution of DFNB21, DFNB24, DFNB29, and DFNB42 loci in autosomal recessive nonsyndromic hearing loss patients in Hormozgan, Iran.

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第一作者： Masoud Akbarzadeh,Laleh

第一单位： Molecular Medicine Research Center, Hormozgan University of Medical Sciences, Bandar Abbas, Iran.

作者： Masoud Akbarzadeh,Laleh ^[1] ; Marzieh,Naseri ^[1] ; Ali Akbar Poursadegh,Zonouzi ^[1] ; Ahmad Poursadegh,Zonouzi ^[2] ; Marjan,Masoudi ^[1] ; Najmeh,Ahangari ^[1] ; Leila,Shams ^[1] ; Azim,Nejatizadeh ^[1]

作者单位： Molecular Medicine Research Center, Hormozgan University of Medical Sciences, Bandar Abbas, Iran. ^[1] Biotechnology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran. ^[2]

关键词 Connexin 30.3 deafness gap junction beta-2 linkage analysis

DOI 10.4103/jrms.JRMS_976_16

PMID 28900455

发布时间 2020-10-01

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Journal of research in medical sciences

2017年22卷

99页

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Diverse pattern of gap junction beta-2 and gap junction beta-4 genes mutations and lack of contribution of DFNB21, DFNB24, DFNB29, and DFNB42 loci in autosomal recessive nonsyndromic hearing loss patients in Hormozgan, Iran.

Journal of research in medical sciences

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Journal of research in medical sciences

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Diverse pattern of gap junction beta-2 and gap junction beta-4 genes mutations and lack of contribution of DFNB21, DFNB24, DFNB29, and DFNB42 loci in autosomal recessive nonsyndromic hearing loss patients in Hormozgan, Iran.

Journal of research in medical sciences

相似文献

Journal of research in medical sciences

相关期刊

检索历史清除