Results 251 to 260 of about 12,927 (274)

Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis

Nature Genetics, 2007
Anneke I Den Hollander, Karsten Boldt, Erwin van Wijk   +2 more
exaly  

New views on RPE65 deficiency: the rod system is the source of vision in a mouse model of Leber congenital amaurosis

Nature Genetics, 2001
Christian Grimm, Eberhart Zrenner, Peter Humphries   +2 more
exaly  

Leber’s Congenital Amaurosis

2009
openaire   +1 more source

Spontaneous activity of opsin apoprotein is a cause of Leber congenital amaurosis

Nature Genetics, 2003
T Michael Redmond, Gordon L Fain
exaly  

Leber congenital amaurosis due to RPE65 mutations and its treatment with gene therapy

Progress in Retinal and Eye Research, 2010
Artur V Cideciyan
exaly  

Leber Congenital Amaurosis

2006
openaire   +1 more source

Safety and Efficacy of Gene Transfer for Leber's Congenital Amaurosis

New England Journal of Medicine, 2008
Francesca Simonelli, Eric A Pierce, Sandro Banfi   +2 more
exaly  

Leber's congenital amaurosis

American Journal of Ophthalmology, 1966
openaire   +1 more source

Effect of Gene Therapy on Visual Function in Leber's Congenital Amaurosis

New England Journal of Medicine, 2008
James W B Bainbridge, Robert Henderson, Andrew Stockman   +2 more
exaly  

Leber's Congenital Amaurosis

2006
openaire   +1 more source