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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.

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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
Language:English
Date:2014
Deposited On:21 Nov 2014 09:34
Last Modified:08 Dec 2017 08:00
Publisher:John Libbey Eurotext
ISSN:1167-1122
Publisher DOI:https://doi.org/10.1684/ejd.2014.2280
PubMed ID:24721395

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