Targeted next-generation sequencing of deafness genes in hearing-impaired individuals uncovers informative mutations. (Q34675175)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24875298%20AND%20SRC:MED&resulttype=core&format=json

19 March 2020

title

Targeted next-generation sequencing of deafness genes in hearing-impaired individuals uncovers informative mutations (English)

1 reference

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19 March 2020

1 reference

1

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19 March 2020

author name string

Tobias Müller

2

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19 March 2020

Indrajit Nanda

3

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19 March 2020

Cordula Neuner

4

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19 March 2020

Michaela A H Hofrichter

5

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19 March 2020

Jörg Schröder

6

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19 March 2020

Oliver Bartsch

7

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19 March 2020

Anne Läßig

8

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19 March 2020

Annerose Keilmann

9

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19 March 2020

Sebastian Schraven

10

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19 March 2020

Fabian Kraus

11

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19 March 2020

Wafaa Shehata-Dieler

12

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19 March 2020

Thomas Haaf

13

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19 March 2020

language of work or name

English

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publication date

29 May 2014

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19 March 2020

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19 March 2020

volume

16

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19 March 2020

issue

12

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19 March 2020

page(s)

945-953

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DFNB16 is a frequent cause of congenital hearing impairment: implementation of STRC mutation analysis in routine diagnostics

19 March 2020

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

7 July 2018

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7 July 2018

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7 July 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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26 October 2018

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7 January 2021

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Identifiers

DOI

10.1038/GIM.2014.65

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release_dqww65stlnf7vfbpx3ivtaetoa

19 March 2020

Fatcat ID

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24 November 2022

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19 March 2020

PubMed publication ID

24875298

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