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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1998 | 1 |
2001 | 1 |
2008 | 1 |
2024 | 0 |
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Four novel mutations in the RPE65 gene in patients with Leber congenital amaurosis.
Hum Mutat. 2001 Aug;18(2):164. doi: 10.1002/humu.1168.
Hum Mutat. 2001.
PMID: 11462243
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.
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Impact of retinal disease-associated RPE65 mutations on retinoid isomerization.
Bereta G, Kiser PD, Golczak M, Sun W, Heon E, Saperstein DA, Palczewski K.
Bereta G, et al.
Biochemistry. 2008 Sep 16;47(37):9856-65. doi: 10.1021/bi800905v. Epub 2008 Aug 23.
Biochemistry. 2008.
PMID: 18722466
Free PMC article.
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