PRCD
Jump to navigation
Jump to search
Lua error in Module:Infobox_gene at line 53: attempt to index field 'wikibase' (a nil value).
Progressive rod-cone degeneration is a protein in humans that is encoded by the PRCD gene. [1]
This gene is predominantly expressed in the retina, and mutations in this gene are the cause of autosomal recessive retinal degeneration in both humans and dogs. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2010].
References
[edit | edit source]- ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
Further reading
[edit | edit source]
 | This article on a gene on human chromosome 17 is a stub. You can help Wikipedia by expanding it. |