Mutations in SAM syndrome and palmoplantar keratoderma patients suggest genotype/phenotype correlations in DSG1 mutations

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Veröffentlicht in:	Journal of the European Academy of Dermatology and Venereology 2022-03, Vol.36 (3), p.e215-e218
Hauptverfasser:	Takeuchi, S., Takeichi, T., Koike, Y., Takama, H., Tanahashi, K., Okuno, Y., Ishii, N., Muro, Y., Ogi, T., Suga, Y., Akiyama, M.
Format:	Artikel
Sprache:	eng
Schlagworte:	Desmoglein 1 - genetics Genetic Association Studies Genotype Humans Keratoderma, Palmoplantar - genetics Mutation Pedigree Phenotype
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creator	Takeuchi, S. Takeichi, T. Koike, Y. Takama, H. Tanahashi, K. Okuno, Y. Ishii, N. Muro, Y. Ogi, T. Suga, Y. Akiyama, M.
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doi_str_mv	10.1111/jdv.17752
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subjects	Desmoglein 1 - genetics Genetic Association Studies Genotype Humans Keratoderma, Palmoplantar - genetics Mutation Pedigree Phenotype
title	Mutations in SAM syndrome and palmoplantar keratoderma patients suggest genotype/phenotype correlations in DSG1 mutations
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