The first AAV-mediated RPE gene therapy to restore visual function was obtained in a canine model of Leber Congenital Amaurosis (LCA), a severe form of autosomal recessive, childhood-onset retinal dystrophy 1;2. Humans with LCA are born with significant vision deficits and usually lose all vision within ten years
<div><h3>Background</h3><p>Leber congenital amaurosis (LCA), a heterogeneous early-onset retinal dys...
LCA is a severe retinal dystrophy characterised by an onset of symptoms before the age of 6 months, ...
Item does not contain fulltextMost genetically distinct inherited retinal degenerations are primary ...
The safety and efficacy of gene therapy for inherited retinal diseases is being tested in humans aff...
The safety and efficacy of gene therapy for inherited retinal diseases is being tested in humans aff...
The safety and efficacy of gene therapy for inherited retinal diseases is being tested in humans aff...
BackgroundMutations in RPE65 cause Leber's congenital amaurosis, a progressive retinal degenerative ...
Leber congenital amaurosis (LCA) is the most severe retinal dystrophy causing blindness or severe vi...
Leber congenital amaurosis (LCA) is a group of autosomal recessive blinding retinal diseases that ar...
Leber congenital amaurosis (LCA) associated with retinal pigment epithelium-specific protein 65 kDa ...
Leber congenital amaurosis (LCA) is the most common inherited cause of blindness in childhood and is...
Leber congenital amaurosis (LCA) is the most common inherited cause of blindness in childhood and is...
BACKGROUND: Leber congenital amaurosis (LCA), a heterogeneous early-onset retinal dystrophy, account...
Leber's congenital amaurosis (LCA) is a group of inherited blinding diseases with onset during child...
none15PURPOSE. To evaluate the suitability of gene delivery-based approaches as potential treatment ...
<div><h3>Background</h3><p>Leber congenital amaurosis (LCA), a heterogeneous early-onset retinal dys...
LCA is a severe retinal dystrophy characterised by an onset of symptoms before the age of 6 months, ...
Item does not contain fulltextMost genetically distinct inherited retinal degenerations are primary ...
The safety and efficacy of gene therapy for inherited retinal diseases is being tested in humans aff...
The safety and efficacy of gene therapy for inherited retinal diseases is being tested in humans aff...
The safety and efficacy of gene therapy for inherited retinal diseases is being tested in humans aff...
BackgroundMutations in RPE65 cause Leber's congenital amaurosis, a progressive retinal degenerative ...
Leber congenital amaurosis (LCA) is the most severe retinal dystrophy causing blindness or severe vi...
Leber congenital amaurosis (LCA) is a group of autosomal recessive blinding retinal diseases that ar...
Leber congenital amaurosis (LCA) associated with retinal pigment epithelium-specific protein 65 kDa ...
Leber congenital amaurosis (LCA) is the most common inherited cause of blindness in childhood and is...
Leber congenital amaurosis (LCA) is the most common inherited cause of blindness in childhood and is...
BACKGROUND: Leber congenital amaurosis (LCA), a heterogeneous early-onset retinal dystrophy, account...
Leber's congenital amaurosis (LCA) is a group of inherited blinding diseases with onset during child...
none15PURPOSE. To evaluate the suitability of gene delivery-based approaches as potential treatment ...
<div><h3>Background</h3><p>Leber congenital amaurosis (LCA), a heterogeneous early-onset retinal dys...
LCA is a severe retinal dystrophy characterised by an onset of symptoms before the age of 6 months, ...
Item does not contain fulltextMost genetically distinct inherited retinal degenerations are primary ...