GEO DataSets

Analysis of retinas of RPE65 null mutants at 2, 4 and 6 months of age. RPE65 is highly expressed in retinal pigment epithelial cells. Mutations in REP65 cause 10-15% of Leber's congenital amaurosis (LCA) cases, a severe form of retinal dystrophy. Results provide insight into early LCA progression.

Organism:

Mus musculus

Type:

Expression profiling by array, transformed count, 3 age, 2 genotype/variation sets

Platform:

GPL1261

Series:

GSE3249

18 Samples

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