Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate. (Q33888425)
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scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate. |
scientific article |
Statements
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate (English)
Haider NB
Cideciyan AV
Swiderski R
Streb LM
Beck G
Hockey R
Hanna DB
Gorman S
Duhl D
Carmi R
Bennett J
Weleber RG
Fishman GA
1 February 2000