(Q50458450)

English

Involvement of DFNB59 mutations in autosomal recessive nonsyndromic hearing impairment.

scientific article published in July 2007

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scholarly article

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Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17373699

Involvement of DFNB59 mutations in autosomal recessive nonsyndromic hearing impairment. (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17373699

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9

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Peter Lichtner

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14 March 2018

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Bernd Wollnik

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Europe PubMed Central

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14 March 2018

http://europepmc.org/abstract/MED/17373699

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Han G Brunner

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14 March 2018

http://europepmc.org/abstract/MED/17373699

Lies H. Hoefsloot

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Lies H Hoefsloot

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14 March 2018

http://europepmc.org/abstract/MED/17373699

Cor W. R. J. Cremers

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Cor W R J Cremers

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http://europepmc.org/abstract/MED/17373699

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Hannie Kremer

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http://europepmc.org/abstract/MED/17373699

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Rob W J Collin

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14 March 2018

http://europepmc.org/abstract/MED/17373699

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Ersan Kalay

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http://europepmc.org/abstract/MED/17373699

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Jaap Oostrik

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http://europepmc.org/abstract/MED/17373699

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Refik Caylan

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http://europepmc.org/abstract/MED/17373699

Anneke den Hollander

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Anneke I den Hollander

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Tim M Strom

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http://europepmc.org/abstract/MED/17373699

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Bayram Toraman

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http://europepmc.org/abstract/MED/17373699

Frans P M Cremers

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Frans P M Cremers

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http://europepmc.org/abstract/MED/17373699

Ahmet Karaguzel

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object named as

Ahmet Karaguzel

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http://europepmc.org/abstract/MED/17373699

author name string

Selçuk Arslan

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14 March 2018

http://europepmc.org/abstract/MED/17373699

Yelda Birinci

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http://europepmc.org/abstract/MED/17373699

publication date

1 July 2007

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Europe PubMed Central

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http://europepmc.org/abstract/MED/17373699

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Europe PubMed Central

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14 March 2018

http://europepmc.org/abstract/MED/17373699

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http://europepmc.org/abstract/MED/17373699

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http://europepmc.org/abstract/MED/17373699

718-723

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Europe PubMed Central

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14 March 2018

http://europepmc.org/abstract/MED/17373699

Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20510

7 January 2021

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Nonsense-mediated mRNA decay in health and disease

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Allegro, a new computer program for multipoint linkage analysis

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https://api.crossref.org/works/10.1002%2FHUMU.20510

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easyLINKAGE-Plus--automated linkage analyses using large-scale SNP data

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https://api.crossref.org/works/10.1002%2FHUMU.20510

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Otoacoustic emissions, their origin in cochlear function, and use.

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https://api.crossref.org/works/10.1002%2FHUMU.20510

7 January 2021

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The potential role of DFNA5, a hearing impairment gene, in p53-mediated cellular response to DNA damage

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20510

7 January 2021

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A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20510

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Non-syndromic, autosomal-recessive deafness

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20510

7 January 2021

based on heuristic

inferred from DOI database lookup

A new locus for autosomal recessive non-syndromal sensorineural hearing impairment (DFNB27) on chromosome 2q23-q31.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20510

7 January 2021

based on heuristic

inferred from DOI database lookup

Auditory neuropathy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20510

7 January 2021

based on heuristic

inferred from DOI database lookup

Nonsyndromic hearing impairment is associated with a mutation in DFNA5

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20510

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/HUMU.20510

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17373699

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17373699

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