(Q27677651)
English
Leber congenital amaurosis 14
Leber congenital amaurosis that has material basis in mutation in the LRAT gene on chromosome 4q31
- LCA14
- Leber Congenital Amaurosis type 14
- Retinal Dystrophy, Early-Onset Severe, Lrat-Related
- Retinitis Pigmentosa, Juvenile, Lrat-Related
- LEBER CONGENITAL AMAUROSIS 14
- LEBER CONGENITAL AMAUROSIS 14; LCA14
Statements
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Identifiers
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