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LEBER CONGENITAL AMAUROSIS 9 (disorder)

Known as: Leber congenital amaurosis, type 9, LEBER CONGENITAL AMAUROSIS 9, LCA9 
National Institutes of Health

Related topics

Related topics

8 relations
Autosomal recessive inheritanceHereditary macular colobomaHyperopiaNMNAT1, ASN273ASP

Broader (1)

Leber Congenital Amaurosis

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Mouse Models of NMNAT 1-Leber Congenital Amaurosis ( LCA 9 ) Recapitulate Key Features of 77 78 79 80 81 82 the Human Disease
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46… 
2015
2015
Characterization of LCA 9-associated NMNAT 1 mutants Characterization of Leber ’ s Congenital Amaurosis-associated NMNAT 1 Mutants
Leber’s congenital amaurosis 9 (LCA9) is an autosomal recessive retinal degeneration condition caused by mutations in the NAD… 
2012
2012
Mutations In Lca9 Cause Human Congenital Blindness Due To Leber Congenital Amaurosis
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… 
2006
2006
Exclusion of LCA5 locus in a consanguineous Turkish family with macular coloboma-type LCA
BackgroundLeber's congenital amaurosis (LCA) is an inherited retinal dystrophy, which causes severe visual impairment in early… 
2003
2003
Identification of LCA9, a New Locus for Leber's Congenital Amaurosis on Chromosome 1p36
1968
1968
[A case of hysteric amaurosis successfully treated by B.A. Gurvich's hypnotic method].
1968
1968
[A case of hysteric amaurosis successfully treated by B.A. Gurvich's hypnotic method].
1956
1956
[Electroencephalographical study of a case of hysteric amaurosis].
1948
1948
Amaurosis y ambliopías histéricas
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