Search Page
Save citations to file
Email citations
Email address has not been verified. Go to
My NCBI account settings
to confirm your email and then refresh this page.
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
| Year | Number of Results |
|---|---|
| 1997 | 1 |
| 1998 | 1 |
| 2001 | 1 |
| 2025 | 0 |
Search Results
3 results
Results by year
Filters applied: . Clear all
Page 1
Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy.
Nat Genet. 1997 Oct;17(2):194-7. doi: 10.1038/ng1097-194.
Nat Genet. 1997.
PMID: 9326941
Promoter analysis of RPE65, the gene encoding a 61-kDa retinal pigment epithelium-specific protein.
Nicoletti A, Kawase K, Thompson DA.
Nicoletti A, et al.
Invest Ophthalmol Vis Sci. 1998 Mar;39(3):637-44.
Invest Ophthalmol Vis Sci. 1998.
PMID: 9501877
Item in Clipboard
Four novel mutations in the RPE65 gene in patients with Leber congenital amaurosis.
Simovich MJ, Miller B, Ezzeldin H, Kirkland BT, McLeod G, Fulmer C, Nathans J, Jacobson SG, Pittler SJ.
Simovich MJ, et al.
Hum Mutat. 2001 Aug;18(2):164. doi: 10.1002/humu.1168.
Hum Mutat. 2001.
PMID: 11462243
Item in Clipboard
Cite
Cite
ARTICLE TYPE
ARTICLE LANGUAGE
AGE
Filters on the sidebar will be reset to the default list and any currently applied filters will be cleared.