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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1997 | 1 |
1998 | 1 |
1999 | 1 |
2002 | 1 |
2009 | 1 |
2010 | 1 |
2024 | 0 |
PubMed (cited) for id: 613829
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Mutation discovered in a feline model of human congenital retinal blinding disease.
Invest Ophthalmol Vis Sci. 2010 Jun;51(6):2852-9. doi: 10.1167/iovs.09-4261. Epub 2010 Jan 6.
Invest Ophthalmol Vis Sci. 2010.
PMID: 20053974
Free PMC article.
Leber congenital amaurosis: clinical correlations with genotypes, gene therapy trials update, and future directions.
Chung DC, Traboulsi EI.
Chung DC, et al.
J AAPOS. 2009 Dec;13(6):587-92. doi: 10.1016/j.jaapos.2009.10.004.
J AAPOS. 2009.
PMID: 20006823
Review.
Item in Clipboard
Novel de novo mutation in CRX gene in a Japanese patient with leber congenital amaurosis.
Nakamura M, Ito S, Miyake Y.
Nakamura M, et al.
Am J Ophthalmol. 2002 Sep;134(3):465-7. doi: 10.1016/s0002-9394(02)01542-8.
Am J Ophthalmol. 2002.
PMID: 12208271
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Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor function.
Swaroop A, Wang QL, Wu W, Cook J, Coats C, Xu S, Chen S, Zack DJ, Sieving PA.
Swaroop A, et al.
Hum Mol Genet. 1999 Feb;8(2):299-305. doi: 10.1093/hmg/8.2.299.
Hum Mol Genet. 1999.
PMID: 9931337
Item in Clipboard
De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis.
Freund CL, Wang QL, Chen S, Muskat BL, Wiles CD, Sheffield VC, Jacobson SG, McInnes RR, Zack DJ, Stone EM.
Freund CL, et al.
Nat Genet. 1998 Apr;18(4):311-2. doi: 10.1038/ng0498-311.
Nat Genet. 1998.
PMID: 9537410
No abstract available.
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Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation.
Furukawa T, Morrow EM, Cepko CL.
Furukawa T, et al.
Cell. 1997 Nov 14;91(4):531-41. doi: 10.1016/s0092-8674(00)80439-0.
Cell. 1997.
PMID: 9390562
Free article.
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