Article ID Journal Published Year Pages File Type
9229552 Journal of Dermatological Science 2005 7 Pages PDF
Abstract
In a patient with severe clinical symptoms, we found two genomic deletions in regions that might be important for function of the ABCC6 transporter. Genomic deletions in ABCC6 may occur more frequently in PXE patients than previously expected and future genetic analysis should focus on these mutations as well.
Related Topics
Health Sciences Medicine and Dentistry Dermatology
Authors
, , , , , , ,