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Epidermolytic hyperkeratosis: clinical update
Epidermolytic hyperkeratosis (EHK), earlier termed as bullous congenital ichthyosiform erythroderma is a skin disorder characterized as an autosomal dominant and rare disorder which has been observed to affect 1 in over 200,000 infants as a consequence of a significant mutation in the genes responsi...
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| Vydáno v: | Clin Cosmet Investig Dermatol |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Dove
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6512611/ https://ncbi.nlm.nih.gov/pubmed/31190940 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/CCID.S166849 |
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