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LEBER CONGENITAL AMAUROSIS 3 (disorder)

Known as: LCA3, Leber Congenital Amaurosis 3 
National Institutes of Health

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2 relations

Broader (2)

Leber Congenital AmaurosisRetinitis Pigmentosa

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Spata 7 is a retinal ciliopathy gene critical for correct RPGRIP 1 localization and protein traf fi cking in the retina
Leber congenital amaurosis (LCA) and juvenile retinitis pigmentosa (RP) are severe hereditary diseases that causes visual… 
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