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- W158841492 abstract "A family is described in which three family members (male propositus, father, and paternal aunt) showed a tritan-like color defect with apparently preferential involvement of the short-wavelength-sensitive (SWS) cone system. Mild macular pigmentary changes were present in two family members and mildly reduced visual acuity in two members. Conventional electroretinography was normal except for delayed implicit times in response to a 30 Hz flickering white light. This condition appears to be a familial macular dystrophy, distinguishable from congenital tritanopia by the presence of morphologic changes in the macula and reduced visual acuity, and differentiated from autosomal-dominant optic atrophy by the absence of clinically detectable optic disc atrophy." @default.
- W158841492 created "2016-06-24" @default.
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- W158841492 date "1989-01-01" @default.
- W158841492 modified "2023-09-24" @default.
- W158841492 title "A Familial Macular Dystrophy with Apparently Preferential Short-Wavelength-Sensitive Cone Involvement. Preliminary Report" @default.
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- W158841492 doi "https://doi.org/10.1007/978-94-009-2695-0_23" @default.
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