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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2005 | 2 |
2006 | 4 |
2007 | 1 |
2024 | 0 |
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Page 1
Compound heterozygous CNGA3 mutations (R436W, L633P) in a Japanese patient with congenital achromatopsia.
Vis Neurosci. 2006 May-Aug;23(3-4):395-402. doi: 10.1017/S095252380623308X.
Vis Neurosci. 2006.
PMID: 16961972
Novel form of a single X-linked visual pigment gene in a unique dichromatic color-vision defect.
Hayashi T, Kubo A, Takeuchi T, Gekka T, Goto-Omoto S, Kitahara K.
Hayashi T, et al. Among authors: goto omoto s.
Vis Neurosci. 2006 May-Aug;23(3-4):411-7. doi: 10.1017/S0952523806233029.
Vis Neurosci. 2006.
PMID: 16961974
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A novel homozygous GRK1 mutation (P391H) in 2 siblings with Oguchi disease with markedly reduced cone responses.
Hayashi T, Gekka T, Takeuchi T, Goto-Omoto S, Kitahara K.
Hayashi T, et al. Among authors: goto omoto s.
Ophthalmology. 2007 Jan;114(1):134-41. doi: 10.1016/j.ophtha.2006.05.069. Epub 2006 Oct 27.
Ophthalmology. 2007.
PMID: 17070587
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Compound heterozygous RDH5 mutations in familial fleck retina with night blindness.
Hayashi T, Goto-Omoto S, Takeuchi T, Gekka T, Ueoka Y, Kitahara K.
Hayashi T, et al. Among authors: goto omoto s.
Acta Ophthalmol Scand. 2006 Apr;84(2):254-8. doi: 10.1111/j.1600-0420.2005.00575.x.
Acta Ophthalmol Scand. 2006.
PMID: 16637847
Free article.
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CYP4V2 mutations in two Japanese patients with Bietti's crystalline dystrophy.
Gekka T, Hayashi T, Takeuchi T, Goto-Omoto S, Kitahara K.
Gekka T, et al. Among authors: goto omoto s.
Ophthalmic Res. 2005 Sep-Oct;37(5):262-9. doi: 10.1159/000087214. Epub 2005 Jul 27.
Ophthalmic Res. 2005.
PMID: 16088246
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Novel NR2E3 mutations (R104Q, R334G) associated with a mild form of enhanced S-cone syndrome demonstrate compound heterozygosity.
Hayashi T, Gekka T, Goto-Omoto S, Takeuchi T, Kubo A, Kitahara K.
Hayashi T, et al. Among authors: goto omoto s.
Ophthalmology. 2005 Dec;112(12):2115. doi: 10.1016/j.ophtha.2005.07.002. Epub 2005 Oct 12.
Ophthalmology. 2005.
PMID: 16225923
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