(Q42738599)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20607074%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

title

Sequence Variations and Haplotypes of the GJB2 Gene Revealed by Resequencing of 192 Chromosomes from the General Population in Korea (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20607074%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20607074%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Hong-Hee Won

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20607074%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

author name string

Hee-Jung Kim

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20607074%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Hee-Jin Kim

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20607074%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Ki-O Lee

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20607074%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Moon-Hee Ko

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20607074%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Hosuk Chu

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20607074%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Yang-Sun Cho

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20607074%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Won-Ho Chung

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20607074%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Jong-Won Kim

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20607074%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Sung Hwa Hong

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20607074%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

language of work or name

1 reference

30 June 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20607074%20AND%20SRC:MED&resulttype=core&format=json

Clinical and Experimental Otorhinolaryngology

7 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20607074%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

volume

3

1 reference

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7 February 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20607074%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

page(s)

65-69

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20607074%20AND%20SRC:MED&resulttype=core&format=json

Creative Commons Attribution-NonCommercial 3.0 Unported

7 February 2020

copyright license

start time

1 January 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

GJB2 mutations and degree of hearing loss: a multicenter study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896735

A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896735

A New Statistical Method for Haplotype Reconstruction from Population Data

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896735

Autosomal recessive nonsyndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delT.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896735

Prevalent connexin 26 gene (GJB2) mutations in Japanese

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896735

Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896735

Connexin-26 mutations in sporadic and inherited sensorineural deafness

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896735

The prevalence of the 235delC GJB2 mutation in a Chinese deaf population.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896735

GJB2 gene mutations in newborns with non-syndromic hearing impairment in Northern China.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896735

Clinical evidence of the nonpathogenic nature of the M34T variant in the connexin 26 gene

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896735

Evidence of a founder effect for the 235delC mutation of GJB2 (connexin�26) in east Asians

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896735

GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896735

Detecting polymorphisms and mutations in candidate genes

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896735

Connexin26 mutations associated with nonsyndromic hearing loss.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896735

Novel mutations in the connexin 26 gene (GJB2) responsible for childhood deafness in the Japanese population.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896735

Genetic epidemiological studies of early-onset deafness in the U.S. school-age population

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896735

GJB2 (connexin 26) mutations are not a major cause of hearing loss in the Indonesian population

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896735

GOLD--graphical overview of linkage disequilibrium

1 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20607074

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Mutation spectrum of the connexin 26 (GJB2) gene in Taiwanese patients with prelingual deafness

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20607074

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.3342/CEO.2010.3.2.65

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20607074%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20607074%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

PubMed publication ID

20607074

1 reference