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Corneal opacity in a heterozygote observed by slit-lamp microscopy
Corneal opacity in a heterozygote observed by slit-lamp microscopy. The corneal involvement results from subepithelial glycosphingolipid deposition. (Reproduced from Sher et al.40 Used by permission.) Source: α-Galactosidase A Deficiency: Fabry Disease, The Online Metabolic and Molecular Bases of Inherited Disease Citation: Valle D, Beaudet AL, Vogelstein B, Kinzler KW, Antonarakis SE, Ballabio A, Gibson K, Mitchell G. The Online Metabolic and Molecular Bases of Inherited Disease; 2014 Available at: Accessed: December 25, 2017 Copyright © 2017 McGraw-Hill Education. All rights reserved
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