ArticleMammalian genome : official journal of the International Mammalian Genome Society2008

A novel mutation in Prph2, a gene regulated by Nr2e3, causes retinal degeneration and outer-segment defects similar to Nr2e3 ( rd7/rd7 ) retinas.

Arne M Nystuen et al.PubMed ↗Full text ↗Publisher ↗

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