Analysis of mitochondrial 12S rRNA A1555G genetic mutation in group of Egyptian children with non-syndromic hearing loss: cross-sectional observational study

被引：0
|
作者：
Hala M. Zeidan [1 ]
Heba Tallah Sherif Abd El Hady [1 ]
Abir Omara [2 ]
Nagwa A. Meguid [1 ]
Mohamed S. Taha [1 ]
机构：
[1] National Research Centre,
[2] Hearing and Speech institute,undefined
来源：
The Egyptian Journal of Otolaryngology | / 41卷 / 1期
关键词：
Hearing loss; Non-syndromic; Mitochondrial mutations; A1555G; Egypt;
D O I：
10.1186/s43163-025-00839-x
中图分类号：
学科分类号：
摘要：
引用
收藏
相关论文
共 27 条
  • [21] Mutation analysis of mitochondrial DNA 12SrRNA and tRNASer(UCN) genes in non-syndromic hearing loss patients
    Konings, Annelies
    Van Camp, Guy
    Goethals, Alain
    Van Eyken, Els
    Vandevelde, Ann
    Ben Azza, Jamila
    Peeters, Nils
    Wuyts, Wim
    Smeets, Hubert
    Van Laer, Lut
    MITOCHONDRION, 2008, 8 (5-6) : 377 - 382
  • [22] Mitochondrial tRNAGlu A14693G variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in a Han Chinese family
    Ding, Yu
    Li, Yongyan
    You, Junyan
    Yang, Li
    Chen, Bobei
    Lu, Jianxin
    Guan, Min-Xin
    JOURNAL OF GENETICS AND GENOMICS, 2009, 36 (04) : 241 - 250
  • [23] Mitochondrial tRNAGlu A14693G variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in a Han Chinese family
    Yu Ding a
    遗传学报, 2009, 36 (04) : 241 - 250
  • [24] Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNASer(UCN) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss
    Yuan, Huijun
    Chen, Jing
    Llu, Xin
    Cheng, Jing
    Wang, Xinjian
    Yang, Li
    Yang, Shuzhi
    Cao, Juyang
    Kang, Dongyang
    Dal, Pu
    Zhai, Suoqlang
    Han, Dongyi
    Young, Wie-Yen
    Guan, Min-Xin
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 362 (01) : 94 - 100
  • [25] Mitochondrial COX2 G7598A Mutation May Have a Modifying Role in the Phenotypic Manifestation of Aminoglycoside Antibiotic-Induced Deafness Associated with 12S rRNA A1555G Mutation in a Han Chinese Pedigree
    Chen, Tianbin
    Liu, Qicai
    Jiang, Ling
    Liu, Can
    Ou, Qishui
    GENETIC TESTING AND MOLECULAR BIOMARKERS, 2013, 17 (02) : 122 - 130
  • [26] Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation
    Wang, QJ
    Li, QZ
    Han, DY
    Zhao, YL
    Zhao, LD
    Qian, YP
    Yuan, H
    Li, RH
    Zhai, SQ
    Young, WY
    Guan, MX
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 340 (02) : 583 - 588
  • [27] Mitochondrial ND5 T12338C, tRNACys T5802C, and tRNAThr G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese pedigrees
    Chen, Bobei
    Sun, Dongmei
    Yang, Li
    Zhang, Chuqin
    Yang, Affen
    Zhu, Yi
    Zhao, Jianyue
    Chen, Yingying
    Guan, Minqiang
    Wang, Xinjian
    Li, Ronghua
    Tang, Xiaowen
    Wang, Jindan
    Tao, Zhihua
    Lu, Jianxin
    Guan, Min-Xin
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2008, 146A (10) : 1248 - 1258
123