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  4. Exome sequencing confirms ZNF408 mutations as a cause of familial retinitis pigmentosa
 
research article

Exome sequencing confirms ZNF408 mutations as a cause of familial retinitis pigmentosa

Habibi, Imen
•
Chebil, Ahmed
•
Kort, Fedra
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2017
Ophthalmic Genetics
  • Details
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Type
research article
DOI
10.1080/13816810.2016.1275020
Web of Science ID

WOS:000415965700017

Author(s)
Habibi, Imen
Chebil, Ahmed
Kort, Fedra
Schorderet, Daniel F.
El Matri, Leila
Date Issued

2017

Publisher

Taylor & Francis Inc

Published in
Ophthalmic Genetics
Volume

38

Issue

5

Start page

494

End page

497

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
SV  
Available on Infoscience
December 4, 2017
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/142490
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