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- W2017076022 abstract "We conducted a ten-year follow-up of an unusual pedigree with an autosomal recessive vitreoretinal degeneration, severe myopia, and congenital encephalocele. All five affected members (four girls and one boy) also had early, recurrent bilateral detachments. Color vision testing disclosed an acquired tritan dyschromatopsia and electroretinography showed subnormal photopic and scotopic amplitudes, delayed b-wave implicit times and 30-Hz flicker-phase relations, and absent scotopic b-wave oscillations." @default.
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- W2017076022 date "1982-07-01" @default.
- W2017076022 modified "2023-09-29" @default.
- W2017076022 title "Autosomal Recessive Vitreoretinopathy and Encephaloceles" @default.
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- W2017076022 doi "https://doi.org/10.1016/0002-9394(82)90185-4" @default.
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