Prenatal human ocular degeneration occurs in Leber's Congenital Amaurosis (LCA1 and 2).
about
Lentiviral expression of retinal guanylate cyclase-1 (RetGC1) restores vision in an avian model of childhood blindnessLeber congenital amaurosis due to RPE65 mutations and its treatment with gene therapyGene Therapy Fully Restores Vision to the All-Cone Nrl(-/-) Gucy2e(-/-) Mouse Model of Leber Congenital Amaurosis-1.AAV-mediated gene therapy in the guanylate cyclase (RetGC1/RetGC2) double knockout mouse model of Leber congenital amaurosis.Determining consequences of retinal membrane guanylyl cyclase (RetGC1) deficiency in human Leber congenital amaurosis en route to therapy: residual cone-photoreceptor vision correlates with biochemical properties of the mutantsInsights gained from gene therapy in animal models of retGC1 deficiency.Leber congenital amaurosis caused by mutations in GUCY2D.
P2860
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P2860
Prenatal human ocular degeneration occurs in Leber's Congenital Amaurosis (LCA1 and 2).
description
2003 nî lūn-bûn
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2003年の論文
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2003年学术文章
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name
Prenatal human ocular degeneration occurs in Leber's Congenital Amaurosis (LCA1 and 2).
@en
type
label
Prenatal human ocular degeneration occurs in Leber's Congenital Amaurosis (LCA1 and 2).
@en
prefLabel
Prenatal human ocular degeneration occurs in Leber's Congenital Amaurosis (LCA1 and 2).
@en
P2093
P50
P1476
Prenatal human ocular degeneration occurs in Leber's Congenital Amaurosis (LCA1 and 2)
@en
P2093
David Hicks
José A Sahel
Noëlle Hanoteau
Sylvain Hanein
P407
P577
2003-01-01T00:00:00Z