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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1997 | 2 |
1998 | 2 |
2008 | 1 |
2024 | 0 |
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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
Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis.
Morimura H, Fishman GA, Grover SA, Fulton AB, Berson EL, Dryja TP.
Morimura H, et al.
Proc Natl Acad Sci U S A. 1998 Mar 17;95(6):3088-93. doi: 10.1073/pnas.95.6.3088.
Proc Natl Acad Sci U S A. 1998.
PMID: 9501220
Free PMC article.
Item in Clipboard
Rpe65 is necessary for production of 11-cis-vitamin A in the retinal visual cycle.
Redmond TM, Yu S, Lee E, Bok D, Hamasaki D, Chen N, Goletz P, Ma JX, Crouch RK, Pfeifer K.
Redmond TM, et al.
Nat Genet. 1998 Dec;20(4):344-51. doi: 10.1038/3813.
Nat Genet. 1998.
PMID: 9843205
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Leber congenital amaurosis: genes, proteins and disease mechanisms.
den Hollander AI, Roepman R, Koenekoop RK, Cremers FP.
den Hollander AI, et al.
Prog Retin Eye Res. 2008 Jul;27(4):391-419. doi: 10.1016/j.preteyeres.2008.05.003. Epub 2008 Jun 1.
Prog Retin Eye Res. 2008.
PMID: 18632300
Review.
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Mutations in RPE65 cause Leber's congenital amaurosis.
Marlhens F, Bareil C, Griffoin JM, Zrenner E, Amalric P, Eliaou C, Liu SY, Harris E, Redmond TM, Arnaud B, Claustres M, Hamel CP.
Marlhens F, et al.
Nat Genet. 1997 Oct;17(2):139-41. doi: 10.1038/ng1097-139.
Nat Genet. 1997.
PMID: 9326927
No abstract available.
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