A novel DFNA5 mutation does not cause hearing loss in an Iranian family. (Q34618064)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17427029 AND SRC:MED&resulttype=core&format=json

29 December 2019

title

A novel DFNA5 mutation does not cause hearing loss in an Iranian family (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17427029 AND SRC:MED&resulttype=core&format=json

29 December 2019

1 reference

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17427029 AND SRC:MED&resulttype=core&format=json

29 December 2019

Kimia Kahrizi

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17427029 AND SRC:MED&resulttype=core&format=json

29 December 2019

Guy Van Camp

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17427029 AND SRC:MED&resulttype=core&format=json

29 December 2019

Richard J Smith

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17427029 AND SRC:MED&resulttype=core&format=json

29 December 2019

author name string

Lut Van Laer

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17427029 AND SRC:MED&resulttype=core&format=json

29 December 2019

Nicole C Meyer

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17427029 AND SRC:MED&resulttype=core&format=json

29 December 2019

Mahdi Malekpour

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17427029 AND SRC:MED&resulttype=core&format=json

29 December 2019

Yasser Riazalhosseini

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17427029 AND SRC:MED&resulttype=core&format=json

29 December 2019

Mahdi Moghannibashi

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17427029 AND SRC:MED&resulttype=core&format=json

29 December 2019

Ann Vandevelde

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17427029 AND SRC:MED&resulttype=core&format=json

29 December 2019

Fatemeh Alasti

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17427029 AND SRC:MED&resulttype=core&format=json

29 December 2019

publication date

11 April 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17427029 AND SRC:MED&resulttype=core&format=json

Journal of Human Genetics

29 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17427029 AND SRC:MED&resulttype=core&format=json

29 December 2019

volume

52

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17427029 AND SRC:MED&resulttype=core&format=json

29 December 2019

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17427029 AND SRC:MED&resulttype=core&format=json

29 December 2019

page(s)

549-552

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17427029 AND SRC:MED&resulttype=core&format=json

A yeast model for the study of human DFNA5, a gene mutated in nonsyndromic hearing impairment.

29 December 2019

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007/S10038-007-0137-2

Is DFNA5 a susceptibility gene for age-related hearing impairment?

21 January 2018

1 reference

12 December 2020

A novel mutation identified in the DFNA5 gene in a Dutch family: a clinical and genetic evaluation

1 reference

12 December 2020

A 3-nucleotide deletion in the polypyrimidine tract of intron 7 of the DFNA5 gene causes nonsyndromic hearing impairment in a Chinese family

1 reference

12 December 2020

Mapping genomic deletions down to the base: a quantitative copy number scanning approach used to characterise and clone the breakpoints of a recurrent 7p14.2p15.3 deletion

1 reference

12 December 2020

Mice lacking Dfna5 show a diverging number of cochlear fourth row outer hair cells

1 reference

12 December 2020

Nonsyndromic hearing impairment is associated with a mutation in DFNA5

1 reference

12 December 2020

DFNA5: hearing impairment exon instead of hearing impairment gene?

1 reference

12 December 2020