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

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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