Allelic heterogeneity among Iranian DFNB7/11 families: report of a new Iranian deaf family with TMC1 mutation identified by next-generation sequencing (Q50353775)

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scientific article published on 25 November 2014

Language	Label	Description	Also known as
English	Allelic heterogeneity among Iranian DFNB7/11 families: report of a new Iranian deaf family with TMC1 mutation identified by next-generation sequencing	scientific article published on 25 November 2014

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

6 March 2018

http://europepmc.org/abstract/MED/25423259

Allelic heterogeneity among Iranian DFNB7/11 families: report of a new Iranian deaf family with TMC1 mutation identified by next-generation sequencing (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 March 2018

http://europepmc.org/abstract/MED/25423259

Javad Tavakkoly-Bazzaz

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25423259 AND SRC:MED&resulttype=core&format=json

9 June 2020

author name string

Elham Davoudi-Dehaghani

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25423259 AND SRC:MED&resulttype=core&format=json

9 June 2020

Mohammad-Sadegh Fallah

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25423259 AND SRC:MED&resulttype=core&format=json

9 June 2020

Hamideh Bagherian

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25423259 AND SRC:MED&resulttype=core&format=json

9 June 2020

Sirous Zeinali

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25423259 AND SRC:MED&resulttype=core&format=json

9 June 2020

language of work or name

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publication date

25 November 2014

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Europe PubMed Central

PubMed publication ID

6 March 2018

http://europepmc.org/abstract/MED/25423259

number of pages

5

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Acta Oto-Laryngologica

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25423259 AND SRC:MED&resulttype=core&format=json

9 June 2020

135

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25423259 AND SRC:MED&resulttype=core&format=json

9 June 2020

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25423259 AND SRC:MED&resulttype=core&format=json

9 June 2020

125-129

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PubMed publication ID

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9 June 2020

describes a project that uses

massive parallel sequencing

1 reference

based on heuristic

inferred from title

Newborn hearing screening--a silent revolution

1 reference

https://api.crossref.org/works/10.3109/00016489.2014.969383

21 January 2018

Autosomal recessive nonsyndromic deafness genes: a review

1 reference

https://api.crossref.org/works/10.3109/00016489.2014.969383

21 January 2018

tmc-1 encodes a sodium-sensitive channel required for salt chemosensation in C. elegans

1 reference

https://api.crossref.org/works/10.3109/00016489.2014.969383

21 January 2018

Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11

1 reference

https://api.crossref.org/works/10.3109/00016489.2014.969383

21 January 2018

Four novel TMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing loss

1 reference

https://api.crossref.org/works/10.3109/00016489.2014.969383

21 January 2018

Identities, frequencies and origins of TMC1 mutations causing DFNB7/B11 deafness in Pakistan

1 reference

https://api.crossref.org/works/10.3109/00016489.2014.969383

21 January 2018

Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function

1 reference

https://api.crossref.org/works/10.3109/00016489.2014.969383

21 January 2018

Novel TMC1 structural and splice variants associated with congenital nonsyndromic deafness in a Sudanese pedigree

1 reference

https://api.crossref.org/works/10.3109/00016489.2014.969383

21 January 2018

Novel sequence variants in the TMC1 gene in Pakistani families with autosomal recessive hearing impairment.

1 reference

https://api.crossref.org/works/10.3109/00016489.2014.969383

21 January 2018

Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: a report of five novel mutations.

1 reference

https://api.crossref.org/works/10.3109/00016489.2014.969383

21 January 2018

TMC1 but not TMC2 is responsible for autosomal recessive nonsyndromic hearing impairment in Tunisian families

1 reference

https://api.crossref.org/works/10.3109/00016489.2014.969383

21 January 2018

Novel compound heterozygous TMC1 mutations associated with autosomal recessive hearing loss in a Chinese family

1 reference

https://api.crossref.org/works/10.3109/00016489.2014.969383

21 January 2018

A transversion mutation in non-coding exon 3 of the TMC1 gene in two ethnically related Iranian deaf families from different geographical regions; evidence for founder effect

1 reference

https://api.crossref.org/works/10.3109/00016489.2014.969383

21 January 2018

Mutations in TMC1 are a common cause of DFNB7/11 hearing loss in the Iranian population.

1 reference

https://api.crossref.org/works/10.3109/00016489.2014.969383

21 January 2018

A novel mutation adjacent to the Bth mouse mutation in the TMC1 gene makes this mouse an excellent model of human deafness at the DFNA36 locus.

1 reference

https://api.crossref.org/works/10.3109/00016489.2014.969383

21 January 2018

Consanguineous marriage in Iran

1 reference

https://api.crossref.org/works/10.3109/00016489.2014.969383

21 January 2018

Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencing.

1 reference

https://api.crossref.org/works/10.3109/00016489.2014.969383

21 January 2018

Identifiers

10.3109/00016489.2014.969383

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25423259 AND SRC:MED&resulttype=core&format=json

9 June 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25423259 AND SRC:MED&resulttype=core&format=json

9 June 2020

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