Khanna et al., 2009 - A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies. Nature Genetics   41(6):739-745 Full text @ Nat. Genet.
3 Genes / Markers
Marker Type Symbol Name
Gene egr2b early growth response 2b
Gene pax2a paired box 2a
Gene rpgrip1l RPGRIP1 like
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.