Frequency of GJB2 mutations in families with autosomal recessive non-syndromic hearing loss in Khuzestan province-Reference-Cited by-同舟云学术

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Frequency of GJB2 mutations in families with autosomal recessive non-syndromic hearing loss in Khuzestan province

Published:2018 Issue:3 Volume:50 Page:837-846
ISSN:0534-0012
Container-title:Genetika
language:en
Short-container-title:Genetika

Author:

Tahmasebi Parisa,Chaleshtori Hashemzadeh Morteza,Abdollahnejad Fatemeh,Alavi Zahra,Sadeghian Ladan,Talebi Farah,Mohammadi-Asl Javad,Saki Nader,Nezhad Seyed,Tabatabaiefar Mohammad

Publisher

National Library of Serbia

Subject

Plant Science,Genetics

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. 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

2. Targeted Drug Delivery in Brain Tumors-nanochemistry Applications and Advances;Current Topics in Medicinal Chemistry;2021-05

3. Nanomedicine and Early Cancer Diagnosis: Molecular Imaging using Fluorescence Nanoparticles;Current Topics in Medicinal Chemistry;2020-12-03

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