Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss (Q34527976)

2 August 2017

title

Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss (English)

1 reference

2 August 2017

1 reference

Qinjun Wei

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2 August 2017

Hongmei Zhu

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2 August 2017

Xuli Qian

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2 August 2017

Zhibin Chen

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2 August 2017

Jun Yao

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2 August 2017

Yajie Lu

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2 August 2017

Xin Cao

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2 August 2017

Guangqian Xing

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2 August 2017

publication date

12 November 2014

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Journal of Translational Medicine

2 August 2017

published in

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2 August 2017

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2 August 2017

page(s)

311

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Creative Commons Attribution 4.0 International

2 August 2017

start time

12 November 2014

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April 2022 Public Data File from Crossref

copyrighted

0 references

cites work

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A novel mutation in the WFS1 gene identified in a Taiwanese family with low-frequency hearing impairment

7 July 2018

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21 January 2018

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PubMed

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inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/S12967-014-0311-1

1 reference

Dimensions Publication ID

2 August 2017

0 references

1 reference

2 August 2017

1 reference