Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9229552 | Journal of Dermatological Science | 2005 | 7 Pages |
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
Evelin Katona, Charalampos Aslanidis, Ãva Remenyik, Márta Csikós, Sarolta Kárpáti, György Paragh, Gerd Schmitz,