Hyperkeratotic cutaneous vascular malformation associated with familial cerebral cavernous malformations (FCCM) with KRIT1/CCM1 mutation
Feldmeyer, L; Baumann-Vogel, H; Tournier-Lasserve, E; Riant, F; Jung, H H; French, L E; Kamarashev, J (2014). Hyperkeratotic cutaneous vascular malformation associated with familial cerebral cavernous malformations (FCCM) with KRIT1/CCM1 mutation. European Journal of Dermatology, 24(2):255-257.
Additional indexing
| Item Type: | Journal Article, refereed, original work |
|---|---|
| Communities & Collections: | 04 Faculty of Medicine > University Hospital Zurich > Clinic for Neurology
04 Faculty of Medicine > University Hospital Zurich > Dermatology Clinic |
| Dewey Decimal Classification: | 610 Medicine & health |
| Scopus Subject Areas: | Health Sciences > Dermatology |
| Language: | English |
| Date: | 2014 |
| Deposited On: | 21 Nov 2014 09:34 |
| Last Modified: | 12 Jan 2025 02:36 |
| Publisher: | John Libbey Eurotext |
| ISSN: | 1167-1122 |
| OA Status: | Green |
| Publisher DOI: | https://doi.org/10.1684/ejd.2014.2280 |
| PubMed ID: | 24721395 |
Permanent URL
https://doi.org/10.5167/uzh-100460
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Feldmeyer, L