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Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor.
Cell. 1997 Nov 14;91(4):543-53. doi: 10.1016/s0092-8674(00)80440-7.
Cell. 1997.
PMID: 9390563
Free article.
A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene.
Sohocki MM, Sullivan LS, Mintz-Hittner HA, Birch D, Heckenlively JR, Freund CL, McInnes RR, Daiger SP.
Sohocki MM, et al.
Am J Hum Genet. 1998 Nov;63(5):1307-15. doi: 10.1086/302101.
Am J Hum Genet. 1998.
PMID: 9792858
Free PMC article.
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