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LEBER CONGENITAL AMAUROSIS 10 (disorder)

Known as: LCA10, Leber Congenital Amaurosis 10 
National Institutes of Health

Related topics

Related topics

2 relations
CEP290 gene

Broader (1)

Leber Congenital Amaurosis

Papers overview

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Highly Cited
2017
Highly Cited
2017
Organizing Section: Biochemistry/Molecular Biology Program Number: 4468 Poster Board Number: B0123 Presentation Time: 11:00 AM–12:45 PM CRISPR/Cas9-Mediated Genome Editing as a Therapeutic Approach…
These abstracts are licensed under a Creative Commons Attribution-NonCommercial-No Derivatives 4.0 International License. Go to… 
2017
2017
Katrine Bosley
Katrine Bosley, CEO of Editas Medicines, discusses the technological tractability of CRISPR, the future of the modality's… 
2016
2016
Mouse Models as Tools to Identify Genetic Pathways for Retinal Degeneration, as Exemplified by Leber's Congenital Amaurosis.
  • B. Chang
  • Methods in molecular biology
  • 2016
  • Corpus ID: 21338718
Leber's congenital amaurosis (LCA) is an inherited retinal degenerative disease characterized by severe loss of vision in the… 
2006
2006
Disease-associated variants of the rod-derived cone viability factor (RdCVF) in Leber congenital amaurosis. Rod-derived cone viability variants in LCA.
Leber congenital amaurosis (LCA) is the most early and severe form of all inherited retinal dystrophies, responsible for… 
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