Molecular diagnosis of <i>SLC26A4</i>-related hereditary hearing loss in a group of patients from two provinces of Iran-Reference-Cited by-同舟云学术

Molecular diagnosis of SLC26A4-related hereditary hearing loss in a group of patients from two provinces of Iran

Published:2021-02-28 Issue:1 Volume:10 Page:23-30
ISSN:2186-361X
Container-title:Intractable & Rare Diseases Research
language:en
Short-container-title:IRDR

Author:

Koohiyan Mahbobeh¹²,Hashemzadeh-Chaleshtori Morteza³,Tabatabaiefar Mohammad Amin¹⁴

Affiliation:

1. Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

2. Cancer Research Center, Shahrekord University of Medical Sciences, Shahrekord, Iran.

3. Cellular and Molecular Research Center, Basic Health Research Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran.

4. Pediatric Inherited Diseases Research Center, Research Institute for Primordial Prevention of Noncommunicable Disease, Isfahan University of Medical Sciences, Isfahan, Iran.

Publisher

International Research and Cooperation Association for Bio & Socio-Sciences Advancement (IRCA-BSSA)

Subject

General Medicine

Link

https://www.jstage.jst.go.jp/article/irdr/10/1/10_2020.03090/_pdf

Reference48 articles.

1. 1. Morton NE. Genetic epidemiology of hearing impairment. Ann N Y Acad Sci. 1991; 630:16-31.

2. 2. Li XC, Everett LA, Lalwani AK, Desmukh D, Friedman TB, Green ED, Wilcox ER. A mutation in PDS causes non-syndromic recessive deafness. Nat Genet. 1998. 18:215-217.

3. 3. Everett LA, Glaser B, Beck JC, Idol JR, Buchs A, Heyman M, Adawi F, Hazani E, Nassir E, Baxevanis AD, Sheffield VC, Green ED. Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS). Nat Genet. 1997; 17:411-422.

4. 4. Albert S, Blons H, Jonard L, et al. SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations. Eur J Hum Genet. 2006; 14:773-779.

5. 5. Koohiyan M. A systematic review of SLC26A4 mutations causing hearing loss in the Iranian population. Int J Pediatr Otorhinolaryngol. 2019. 125:1-5.

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