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Arq. Bras. Oftalmol. 2024; 87 (5):

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PRPH2 mutation c.582-1G>A causing adult-onset macular dystrophy with a benign concentric annular macular dystrophy phenotype in a family

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Mutação c.582-1G>A do gene PRPH2 causando distrofia macular de início adulto com fenótipo de distrofia macular anular concêntrica benigna em uma família. Arq. Bras. Oftalmol. 2024;87(5):.
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