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

Anand Swaroop, Qing Liang Wang, Weiping Wu, Jason Cook, Caraline Coats, Siqun Xu, Shiming Chen, Donald J. Zack, Paul A. Sieving

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Medicine & Life Sciences