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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

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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
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