AAAAAA

   
Results: 1-1 |
Results: 1
Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for theinvolvement of CRX in the development of photoreceptor function
Authors: Swaroop, A Wang, QL Wu, WP Cook, J Coats, C Xu, SQ Chen, SM Zack, DJ Sieving, PA
Citation: A. Swaroop et al., Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for theinvolvement of CRX in the development of photoreceptor function, HUM MOL GEN, 8(2), 1999, pp. 299-305
Risultati: 1-1 |