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
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| Description | scientific article |
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author: Anand Swaroop Don Zack |
| Publication date | February 1, 1999 |
| Language | English |
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