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rainer schmuth
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Rainer Schruth
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Morphological alterations in two siblings with autosomal recessive congenital ichthyosis associated with CYP4F22 mutations.
Br J Dermatol. 2017 Apr;176(4):1068-1073. doi: 10.1111/bjd.14860. Epub 2017 Jan 17.
Br J Dermatol. 2017.
PMID: 27449533
Free article.
Expression of the C-C chemokine MIP-3 alpha/CCL20 in human epidermis with impaired permeability barrier function.
Schmuth M, Neyer S, Rainer C, Grassegger A, Fritsch P, Romani N, Heufler C.
Schmuth M, et al.
Exp Dermatol. 2002 Apr;11(2):135-42. doi: 10.1034/j.1600-0625.2002.110205.x.
Exp Dermatol. 2002.
PMID: 11994140
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