| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 3188407 | Annales de Dermatologie et de Vénéréologie | 2010 | 7 Pages |
Abstract
Our study of this family confirmed the classical characteristics of KPP-BFB as well as demonstrating several associated clinical signs of which the significance will be determined in subsequent studies. Further screening studies to identify mutated genes in the region of interest will help us to understand the molecular basis of this disease and hopefully to propose suitable treatment.
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Authors
I. El Amri, O. Mamai, N. Ghariani, M. Denguezli, B. Sriha, L. Adala, A. Saad, M. Gribaa, R. Nouira,