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Mild case of congenital ichthyosiform erythroderma with periodic exacerbation: Novel mutations in ABCA12 and upregulation of calprotectin in the epidermis.

AuthorsYoshihiro Wada, Minori Kusakabe, Makoto Nagai, Masaaki Yamamoto, Yasutomo Imai, Yoshi-Hiro Ide, Seiichi Hirota, Kiyofumi Yamanishi
JournalThe Journal of dermatology (J Dermatol) Vol. 44 Issue 11 Pg. e282-e283 (Nov 2017) ISSN: 1346-8138 [Electronic] England
PMID28771802 (Publication Type: Case Reports, Letter)
Chemical References
  • ABCA12 protein, human
  • ATP-Binding Cassette Transporters
  • Leukocyte L1 Antigen Complex
Topics
  • ATP-Binding Cassette Transporters (genetics)
  • Child, Preschool
  • Epidermis (metabolism, ultrastructure)
  • Female
  • Humans
  • Ichthyosiform Erythroderma, Congenital (genetics, metabolism, pathology)
  • Leukocyte L1 Antigen Complex (metabolism)

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