A novel mutation in the ARS (component B) gene encoding SLURP-1 in a Turkish family with mal de Meleda
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.2006.07288.x/fullpdf
Reference8 articles.
1. Ueber Keratoma hereditarium;Neumann;Arch Derm Syph,1898
2. Clinical and genetic studies of 3 large, consanguineous, Algerian families with mal de Meleda;Bouadjar;Arch Dermatol,2000
3. Identification of recurrent mutations in the ARS (component B) gene encoding SLURP-1 in two families with mal de Meleda;Ward;J Invest Dermatol,2003
4. Mal de Meleda keratoderma with pseudoainhum;Bergman;Br J Dermatol,1993
5. Mutations in the gene encoding SLURP-1 in mal de Meleda;Fischer;Hum Mol Genet,2001
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3. Novel nonsense variants in SLURP1 and DSG1 cause palmoplantar keratoderma in Pakistani families;BMC Medical Genetics;2019-08-23
4. Identification of novel homozygous SLURP1 mutation in a Javanese family with Mal de Meleda;International Journal of Dermatology;2017-10-11
5. Knowledge, perception, and practice of patients about pityriasis versicolor in Kaduna, North Central Nigeria;International Journal of Dermatology;2017-05-31
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