A mutation in CRX causing pigmented paravenous retinochoroidal atrophy

Oh, J. K., Nuzbrokh, Y., Lee, W., Lima de Carvalho, J. R., Wang, N. K., Sparrow, J. R., Allikmets, R., & Tsang, S. H. (2020). A mutation in CRX causing pigmented paravenous retinochoroidal atrophy. European Journal of Ophthalmology, 32(1), NP235–NP239. https://doi.org/10.1177/1120672120957599
Authors:
Jin Kyun Oh
Yan Nuzbrokh
Winston Lee
Jose Ronaldo Lima de Carvalho
Nan Kai Wang
Janet R Sparrow
Rando Allikmets
Stephen H Tsang
Affiliated Authors:
Winston Lee
Nan Kai Wang
Janet R Sparrow
Rando Allikmets
Stephen H Tsang
Columbia Affiliation:
Author Keywords:
crx
inherited retinal dystrophy
pigmented paravenous retinochoroidal atrophy
rod-cone dystrophy
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Publication Type:
Article
Unique ID:
10.1177/1120672120957599
PMID:
32927963
DOI:
10.1177/1120672120957599
Journal:
European Journal of Ophthalmology
Publication Date:
Data Source:
Scopus
Source Link:
View Scopus Record

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