(Q27677710)
English
Leber congenital amaurosis 10
A Leber congenital amaurosis that is characterized by severe infantile-onset cone-rod dystrophy with high hyperopia and severe ERG abnormalities and has material basis in mutation in the CEP290 gene on chromosome 12q21.32.
- LCA10
- Leber Congenital Amaurosis type 10
- Amaurosis congenita of Leber, type 10
- LEBER CONGENITAL AMAUROSIS 10
- LEBER CONGENITAL AMAUROSIS 10; LCA10
Statements
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Identifiers
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