Coinheritance of biallelic SLURP1 and SLC39A4 mutations cause a severe genodermatosis with skin peeling and hair loss all over the body

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Item Type:	Letter
Title:	Coinheritance of biallelic SLURP1 and SLC39A4 mutations cause a severe genodermatosis with skin peeling and hair loss all over the body
Creators Name:	Harms, F.L., Nampoothiri, S., Kortüm, F., Thomas, J., Panicker, V.V., Alawi, M., Altmüller, J., Yesodharan, D. and Kutsche, K.
Keywords:	Alopecia, Biopsy, Cation Transport Proteins, Consanguinity, DNA Mutational Analysis, Exfoliative Dermatitis, Exome Sequencing, Ly Antigens, Mutation, Palmoplantar Keratoderma, Skin, Urokinase-Type Plasminogen Activator
Source:	British Journal of Dermatology
ISSN:	0007-0963
Publisher:	Wiley
Volume:	179
Number:	5
Page Range:	1192-1194
Date:	1 November 2018
Official Publication:	https://doi.org/10.1111/bjd.16912
PubMed:	View item in PubMed

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