Corneal involvement in a case of autosomal dominant Stargardt-like macular dystrophy (STGD3) with ELOVL4 mutation
2020
Stargardt-like macular dystrophy (STGD3) represents an early onset, autosomal dominant form of macular degeneration. Genetic studies revealed that STGD3 is caused by mutations in the ELOngation of ...
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