Prevalence of mutations in GJB2, SLC26A4, and mtDNA in children with severe or profound sensorineural hearing loss in southwestern China. (Q34779797)

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24 February 2020

title

Prevalence of mutations in GJB2, SLC26A4, and mtDNA in children with severe or profound sensorineural hearing loss in southwestern China (English)

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24 February 2020

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sensorineural hearing loss

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13

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24 February 2020

author name string

Jie Qing

1

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24 February 2020

Yuan Zhou

2

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24 February 2020

Ruosha Lai

3

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24 February 2020

Peng Hu

4

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24 February 2020

Yan Ding

5

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24 February 2020

Weijing Wu

6

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24 February 2020

Zian Xiao

7

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24 February 2020

Phi T Ho

8

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24 February 2020

Yuyuan Liu

9

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24 February 2020

Jia Liu

10

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24 February 2020

Lilin Du

11

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24 February 2020

Denise Yan

12

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24 February 2020

Xuezhong Liu

14

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24 February 2020

Dinghua Xie

15

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24 February 2020

publication date

1 January 2015

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Genetic Testing and Molecular Biomarkers

24 February 2020

published in

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24 February 2020

volume

19

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24 February 2020

issue

1

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24 February 2020

page(s)

52-58

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Restudy of malformations of the internal auditory meatus, cochlear nerve canal and cochlear nerve

24 February 2020

cites work

1 reference

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Genetic mutations in nonsyndromic deafness patients of Chinese minority and Han ethnicities in Yunnan, China

7 July 2018

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Molecular and clinical characterization of the variable phenotype in Korean families with hearing loss associated with the mitochondrial A1555G mutation

7 July 2018

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Common molecular etiologies are rare in nonsyndromic Tibetan Chinese patients with hearing impairment

7 July 2018

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Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G, GJB2, and SLC26A4 mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China

7 July 2018

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Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China

7 July 2018

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Molecular analysis of the GJB2, GJB6 and SLC26A4 genes in Korean deafness patients

7 July 2018

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Newborn hearing screening--a silent revolution

7 July 2018

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Sensorineural hearing loss in children.

7 July 2018

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Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family

7 July 2018

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Molecular genetics of hearing loss

7 July 2018

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Cx26 deafness: mutation analysis and clinical variability

7 July 2018

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A mutation in PDS causes non-syndromic recessive deafness

7 July 2018

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Prevalence of GJB2 mutations in the Silk Road region of China and a report of three novel variants

7 July 2018

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Common molecular etiology of patients with nonsyndromic hearing loss in Tibetan, Tu nationality, and Mongolian patients in the northwest of China

26 October 2018

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Microarray-based mutation detection of pediatric sporadic nonsyndromic hearing loss in China

26 October 2018

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Study of mtDNA 12S rRNA A1555G, GJB2, GJB3 gene mutation in Uighur and Han people with hereditary nonsyndromic hearing loss in Xinjiang

26 October 2018

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Comparative analysis of the recurrent mutations between Uigur and Han ethnic deaf group in Xinjiang region of China

26 October 2018

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Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss

26 October 2018

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Molecular analysis of mitochondrial gene mutations in Korean patients with nonsyndromic hearing loss.

26 October 2018

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GJB2, SLC26A4 and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects

26 October 2018

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A distinct spectrum of SLC26A4 mutations in patients with enlarged vestibular aqueduct in China

26 October 2018

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SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations

26 October 2018

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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

26 October 2018

1 reference

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The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population

26 October 2018

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High frequency hearing loss correlated with mutations in the GJB2 gene

26 October 2018

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Mitochondrial ribosomal RNA mutation associated with both antibiotic–induced and non–syndromic deafness

26 October 2018

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26 October 2018

Identifiers

DOI

10.1089/GTMB.2014.0241

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25493717 AND SRC:MED&resulttype=core&format=json

24 February 2020

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24 February 2020

PubMed publication ID

25493717

1 reference