Anderson–Fabry disease: Clinical manifestations of disease in female heterozygotes
- 1 November 2001
- journal article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 24 (7), 715-724
- https://doi.org/10.1023/a:1012993305223
Abstract
Anderson–Fabry disease is a rare, X-chromosomal lipid storage disorder caused by a deficiency of lysosomal α-galactosidase A. Clinical manifestations of Anderson–Fabry disease include excruciating...Keywords
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