Schnyder corneal dystrophy-associated UBIAD1 is defective in MK-4 synthesis and resists autophagy-mediated degradation
Author:
Funder
National Institutes of Health
Publisher
Elsevier BV
Subject
Cell Biology,Endocrinology,Biochemistry
Reference51 articles.
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2. Mutations in the UBIAD1 gene, encoding a potential prenyltransferase, are causal for Schnyder crystalline corneal dystrophy;Orr;PLoS One.,2007
3. Mutations in the UBIAD1 gene on chromosome short arm 1, region 36, cause Schnyder crystalline corneal dystrophy;Weiss;Invest. Ophthalmol. Vis. Sci.,2007
4. Visual morbidity in thirty-four families with Schnyder crystalline corneal dystrophy (an American Ophthalmological Society thesis);Weiss;Trans. Am. Ophthalmol. Soc.,2007
5. Bringing bioactive compounds into membranes: the UbiA superfamily of intramembrane aromatic prenyltransferases;Li;Trends Biochem. Sci.,2016
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