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A p.478I>T KRT1 mutation in a case of annular epidermolytic ichthyosis
Annular epidermolytic ichthyosis (AEI; Online Mendelian Inheritance in Man [OMIM]# 607602) is a rare subtype of epidermolytic ichthyosis that is characterized by polycyclic, migratory erythematous and scaly plaques. It typically results from dominant mutations in the keratin 1 or keratin 10 genes. W...
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| Yayımlandı: | Pediatr Dermatol |
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| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2018
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7903949/ https://ncbi.nlm.nih.gov/pubmed/30152556 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/pde.13643 |
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