Haplotype analysis in western European patients with mal de Meleda: founder effect for the W15R mutation in theSLURP1gene
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjd.12203/fullpdf
Reference10 articles.
1. Mutations in the gene encoding SLURP-1 in Mal de Meleda;Fischer;Hum Mol Genet,2001
2. Identification of SLURP-1 as an epidermal neuromodulator explains the clinical phenotype of mal de Meleda;Chimienti;Hum Mol Genet,2003
3. SLURP1 is a late marker of epidermal differentiation and is absent in mal de Meleda;Favre;J Invest Dermatol,2007
4. A novel missense mutation in the gene encoding SLURP-1 in patients with mal de Meleda from northern Tunisia;Charfeddine;Br J Dermatol,2003
5. Novel mutations in the gene encoding secreted lymphocyte antigen-6/urokinase-type plasminogen activator receptor-related protein-1 (SLURP-1) and description of five ancestral haplotypes in patients with mal de Meleda;Marrakchi;J Invest Dermatol,2003
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2. Phenotypic Variability with SLURP1 Mutations and Diffuse Palmoplantar Keratoderma;Acta Dermato Venereologica;2020
3. Identification of novel homozygous SLURP1 mutation in a Javanese family with Mal de Meleda;International Journal of Dermatology;2017-10-11
4. Knowledge, perception, and practice of patients about pityriasis versicolor in Kaduna, North Central Nigeria;International Journal of Dermatology;2017-05-31
5. Inherited Disorders of Cornification;Rook's Textbook of Dermatology, Ninth Edition;2016-10-09
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