可变性红斑角化病。三例报告并文献复习 - Suppr

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Erythrokeratodermia variabilis. Report of three cases and review of the literature.

作者信息

Brown J, Kierland R R

出版信息

Arch Dermatol. 1966 Feb;93(2):194-201. doi: 10.1001/archderm.93.2.194.

DOI:10.1001/archderm.93.2.194

PMID:4159396

Abstract

摘要

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引用本文的文献

The molecular pathology of progressive symmetric erythrokeratoderma: a frameshift mutation in the loricrin gene and perturbations in the cornified cell envelope.进行性对称性红斑角皮病的分子病理学：loricrin基因中的移码突变与角质化细胞包膜的紊乱

Am J Hum Genet. 1997 Sep;61(3):581-9. doi: 10.1086/515518.

Genetic linkage between erythrokeratodermia variabilis and Rh locus.变异性红斑角皮症与Rh血型位点之间的遗传连锁

Hum Genet. 1984;68(2):165-8. doi: 10.1007/BF00279308.

Epidermal Langerhans cells in erythrokeratodermia variabilis. Histochemical and ultrastructural investigations before and after treatment with etretinate (RO 10-9359).

Arch Dermatol Res. 1982;274(3-4):339-48. doi: 10.1007/BF00403739.

[Variable erythrokeratodermias. Enzyme histochemical and autoradiographic studies in 2 cases].

Arch Klin Exp Dermatol. 1969;235(3):241-51.

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