Identification of an oncostatin M receptor mutation associated with familial primary cutaneous amyloidosis

Babilas, P., Fiebig, B. S., Aslanidis, C., Hansen, J., Röcken, C., Schröder, J., Schmitz, G., Weber, B. H. F., Landthaler, M. and Vogt, T. (2009) Identification of an oncostatin M receptor mutation associated with familial primary cutaneous amyloidosis British Journal of Dermatology, 161 (4). pp. 944-947. DOI 10.1111/j.1365-2133.2009.09237.x.

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Supplementary data:

Document Type: Article
Keywords: amyloidosischromosome 5 genetic linkage heterozygous missense mutation osmr gene multiple endocrine neoplasia lichen amyloidosis epidermal-keratinocytes skin generations activation type-2a cells
Research affiliation: OceanRep > The Future Ocean - Cluster of Excellence
Kiel University
Refereed: Yes
DOI etc.: 10.1111/j.1365-2133.2009.09237.x
ISSN: 0007-0963
Projects: Future Ocean
Date Deposited: 11 Feb 2011 12:15
Last Modified: 27 Jan 2012 06:00
URI: http://eprints.uni-kiel.de/id/eprint/9278

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