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Conference item

The retinal phenotype associated with the frequent, synonymous c.783G > A mutation in CDHR1

Publication status:
Published
Peer review status:
Reviewed (other)

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Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Oxford college:
Merton College
Role:
Author
ORCID:
0000-0002-0424-5852
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Name:
Medical Research Council
Grant:
MR/R000735/1
Publisher:
Association for Research in Vision and Ophthalmology
Host title:
Investigative Ophthalmology and Visual Science
Journal:
Investigative Ophthalmology and Visual Science More from this journal
Volume:
59
Issue:
9
Pages:
3146
Publication date:
2018-07-01
EISSN:
1552-5783
ISSN:
0146-0404
Language:
English
Keywords:
Pubs id:
926175
Local pid:
pubs:926175
Deposit date:
2020-07-09

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