Associated Papers
Stargardt Disease Due to an Intronic Mutation in the ABCA4: A Case Report.
Lugo-Merly A et al.
International Medical Case Reports Journal, 2022
The genetic architecture of Stargardt macular dystrophy (STGD1): a longitudinal 40-year study in a genetic isolate.
Green JS et al.
European Journal of Human Genetics : Ejhg, 2020
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