Pseudoxanthoma elasticum (PXE), a prototypic heritable disorder with ectopic mineralization, manifests with characteristic skin findings, ocular involvement, and cardiovascular problems. The classic forms of PXE are due to loss-of-function mutations in the ABCC6 gene, which encodes ABCC6, a putative
Researching the biology of PXE: Partnering in the process
โ Scribed by Terry, Sharon F. ;Boyd, Charles D.
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 190 KB
- Volume
- 106
- Category
- Article
- ISSN
- 0148-7299
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