Frequency of GJB 2 mutations, GJB 6‐D13S1830 and GJB 6‐D13S1854 deletions among patients with non‐syndromic hearing loss from the central region of Iran-Reference-Cited by-同舟云学术

Frequency of GJB 2 mutations, GJB 6‐D13S1830 and GJB 6‐D13S1854 deletions among patients with non‐syndromic hearing loss from the central region of Iran

Published:2019-06-04 Issue:7 Volume:7 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Naddafnia Hossein¹,Noormohammadi Zahra¹^ORCID,Irani Shiva¹,Salahshoorifar Iman¹

Affiliation:

1. Department of Biology, Science and Research Branch Islamic Azad University Tehran Iran

Funder

Islamic Azad University

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.780

Reference36 articles.

1. Prevalent connexin 26 gene (GJB2) mutations in Japanese

2. Connexin mutations in Brazilian patients with skin disorders with or without hearing loss

3. Mutation Analysis of FamilialGJB2-Related Deafness in Iranian Azeri Turkish Patients

4. Prevalence of IVS1+1G>A mutation among Iranian Azeri Turkish patients with autosomal recessive non-syndromic hearing loss (ARNSHL)

5. A study of GJB2 and delGJB6-D13S1830 mutations in Brazilian non-syndromic deaf children from the Amazon region

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3. A systematic review of the monogenic causes of Non‐Syndromic Hearing Loss (NSHL) and discussion of Current Diagnosis and Treatment options;Clinical Genetics;2022-09-29

4. GJB2 mutations in Iranian Azeri population with autosomal recessive nonsyndromic hearing loss (ARNSHL): First report of c.238 C>A mutation in Iran;Journal of Clinical Laboratory Analysis;2021-09-28

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