Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor function (Q28296223)
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scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor function |
scientific article |
Statements
Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor function (English)
Q L Wang
W Wu
J Cook
C Coats
S Xu
S Chen
1 February 1999