Increased cone sensitivity to ABCA4 deficiency provides insight into macular vision loss in Stargardt's dystrophy.
about
The Y141C knockin mutation in RDS leads to complex phenotypes in the mouse.Natural history of cone disease in the murine model of Leber congenital amaurosis due to CEP290 mutation: determining the timing and expectation of therapy.Gene Therapy of ABCA4-Associated Diseases.Clinical and molecular characteristics of childhood-onset Stargardt disease.DNA nanoparticle-mediated ABCA4 delivery rescues Stargardt dystrophy in mice.Lipofuscin and A2E accumulate with age in the retinal pigment epithelium of Nrl-/- miceEffective delivery of large genes to the retina by dual AAV vectors.Retinal phenotypic characterization of patients with ABCA4 retinopathydue to the homozygous p.Ala1773Val mutation.Early Patterns of Macular Degeneration in ABCA4-Associated Retinopathy.
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P2860
Increased cone sensitivity to ABCA4 deficiency provides insight into macular vision loss in Stargardt's dystrophy.
description
2011 nî lūn-bûn
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2011年の論文
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2011年論文
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2011年論文
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2011年論文
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2011年論文
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2011年論文
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2011年论文
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2011年论文
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2011年论文
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name
Increased cone sensitivity to ...... loss in Stargardt's dystrophy.
@ast
Increased cone sensitivity to ...... loss in Stargardt's dystrophy.
@en
type
label
Increased cone sensitivity to ...... loss in Stargardt's dystrophy.
@ast
Increased cone sensitivity to ...... loss in Stargardt's dystrophy.
@en
prefLabel
Increased cone sensitivity to ...... loss in Stargardt's dystrophy.
@ast
Increased cone sensitivity to ...... loss in Stargardt's dystrophy.
@en
P2093
P2860
P1476
Increased cone sensitivity to ...... loss in Stargardt's dystrophy.
@en
P2093
Janet R Sparrow
Muna I Naash
Rasha Makkia
Shannon M Conley
P2860
P304
P356
10.1016/J.BBADIS.2011.10.007
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P577
2011-10-13T00:00:00Z