Molecular diagnosis of <i>SLC26A4</i>-related hereditary hearing loss in a group of patients from two provinces of Iran.

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作者： Mahbobeh,Koohiyan ^[1] ; Morteza,Hashemzadeh-Chaleshtori ^[2] ; Mohammad Amin,Tabatabaiefar ^[3]

作者单位： Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran. ^[1] Cancer Research Center, Shahrekord University of Medical Sciences, Shahrekord, Iran. ^[2] Cellular and Molecular Research Center, Basic Health Research Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran. ^[3] Pediatric Inherited Diseases Research Center, Research Institute for Primordial Prevention of Noncommunicable Disease, Isfahan University of Medical Sciences, Isfahan, Iran. ^[4]

关键词 Iran Pendred syndrome SLC26A4 autosomal recessive non-syndromic hearing loss

DOI 10.5582/irdr.2020.03090

PMID 33614372

发布时间 2021-02-23

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Intractable & rare diseases research

2021年10卷1期

23-30页

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Molecular diagnosis of <i>SLC26A4</i>-related hereditary hearing loss in a group of patients from two provinces of Iran.

Intractable & rare diseases research

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Intractable & rare diseases research

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Molecular diagnosis of <i>SLC26A4</i>-related hereditary hearing loss in a group of patients from two provinces of Iran.

Intractable & rare diseases research

相似文献

Intractable & rare diseases research

相关期刊

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