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Title
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.
Authors
Swaroop A; Wang QL; Wu W; Cook J; Coats C; Xu S; Chen S; Zack DJ; Sieving PA
Publication
Human molecular genetics, 1999, Vol 8, Issue 2, p299