(Q35204053)

7 August 2017

title

A rare novel mutation in TECTA causes autosomal dominant nonsyndromic hearing loss in a Mongolian family (English)

1 reference

7 August 2017

0 references

1 reference

Haihua Bai

1

1 reference

7 August 2017

Xukui Yang

2

1 reference

7 August 2017

Temuribagen

3

1 reference

7 August 2017

Guilan

4

1 reference

7 August 2017

Suyalatu

5

1 reference

7 August 2017

Narisu

6

1 reference

7 August 2017

Huiguang Wu

7

1 reference

7 August 2017

Yujie Chen

8

1 reference

7 August 2017

Yangjian Liu

9

1 reference

7 August 2017

Qizhu Wu

10

1 reference

7 August 2017

publication date

19 March 2014

1 reference

7 August 2017

1 reference

7 August 2017

volume

15

1 reference

7 August 2017

page(s)

34

1 reference

Three deaf mice: mouse models for TECTA-based human hereditary deafness reveal domain-specific structural phenotypes in the tectorial membrane

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994966

DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994966

Deficient forward transduction and enhanced reverse transduction in the alpha tectorin C1509G human hearing loss mutation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994966

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994966

Audiological evaluation of affected members from a Dutch DFNA8/12 (TECTA) family

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994966

A novel TECTA mutation in a Dutch DFNA8/12 family confirms genotype-phenotype correlation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994966

Newborn hearing screening--a silent revolution

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994966

A deafness mutation isolates a second role for the tectorial membrane in hearing

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994966

Human Nonsyndromic Sensorineural Deafness

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994966

Association of clinical features with mutation of TECTA in a family with autosomal dominant hearing loss

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994966

A cysteine substitution in the zona pellucida domain of alpha-tectorin results in autosomal dominant, postlingual, progressive, mid frequency hearing loss in a Spanish family

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994966

Alpha-tectorin involvement in hearing disabilities: one gene--two phenotypes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994966

Mutation in the zonadhesin-like domain of alpha-tectorin associated with autosomal dominant non-syndromic hearing loss.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994966

Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment

28 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-15-34

A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-15-34

Mapping of the alpha-tectorin gene (TECTA) to mouse chromosome 9 and human chromosome 11: a candidate for human autosomal dominant nonsyndromic deafness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-15-34

A targeted deletion in alpha-tectorin reveals that the tectorial membrane is required for the gain and timing of cochlear feedback.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-15-34

TECTA mutations in Japanese with mid-frequency hearing loss affected by zona pellucida domain protein secretion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-15-34

21 January 2018

Identifiers

DOI

10.1186/1471-2350-15-34

1 reference

Dimensions Publication ID

7 August 2017

0 references

1 reference

7 August 2017

1 reference