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- W2413012839 abstract "Two German siblings were found to suffer from night blindness and mild retinal dystrophy but no other clinical symptoms of vitamin A deficiency. Even though they had no detectable plasma retinal-binding protein (RBP) and their plasma retinol was exceedingly low, they showed normal physiologic functions and growth. Their RBP gene was found to harbor two point mutations. Their post-prandial plasma levels of retinyl esters were normal, and it is likely that they derived their tissue retinol from retinyl esters." @default.
- W2413012839 created "2016-06-24" @default.
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- W2413012839 date "2009-04-27" @default.
- W2413012839 modified "2023-09-26" @default.
- W2413012839 title "A Case of Human Vitamin A Deficiency Caused by an Inherited Defect in Retinol-Binding Protein Without Clinical Symptoms Except Night Blindness" @default.
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- W2413012839 doi "https://doi.org/10.1111/j.1753-4887.1999.tb06955.x" @default.
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