Universität zu Köln

Harms, F. L., Nampoothiri, S., Kortuem, F., Thomas, J., Panicker, V. V., Alawi, M., Altmueller, J., Yesodharan, D. and Kutsche, K. (2018). Coinheritance of biallelic SLURP1 and SLC39A4 mutations cause a severe genodermatosis with skin peeling and hair loss all over the body. Br. J. Dermatol., 179 (5). S. 1192 - 1195. HOBOKEN: WILEY. ISSN 1365-2133

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Item Type:	Journal Article
Creators:	Creators Email ORCID ORCID Put Code Harms, F. L. UNSPECIFIED UNSPECIFIED UNSPECIFIED Nampoothiri, S. UNSPECIFIED UNSPECIFIED UNSPECIFIED Kortuem, F. UNSPECIFIED UNSPECIFIED UNSPECIFIED Thomas, J. UNSPECIFIED UNSPECIFIED UNSPECIFIED Panicker, V. V. UNSPECIFIED UNSPECIFIED UNSPECIFIED Alawi, M. UNSPECIFIED UNSPECIFIED UNSPECIFIED Altmueller, J. UNSPECIFIED UNSPECIFIED UNSPECIFIED Yesodharan, D. UNSPECIFIED UNSPECIFIED UNSPECIFIED Kutsche, K. UNSPECIFIED UNSPECIFIED UNSPECIFIED
URN:	urn:nbn:de:hbz:38-167831
DOI:	10.1111/bjd.16912
Journal or Publication Title:	Br. J. Dermatol.
Volume:	179
Number:	5
Page Range:	S. 1192 - 1195
Date:	2018
Publisher:	WILEY
Place of Publication:	HOBOKEN
ISSN:	1365-2133
Language:	English
Faculty:	Unspecified
Divisions:	Unspecified
Subjects:	no entry
Uncontrolled Keywords:	Keywords Language ACRODERMATITIS-ENTEROPATHICA; GENE; MELEDA Multiple languages Dermatology Multiple languages
Refereed:	Yes
URI:	http://kups.ub.uni-koeln.de/id/eprint/16783