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Netherton Syndrome in One Chinese Adult with a Novel Mutation in the SPINK5 Gene and Immunohistochemical Studies of LEKTI
BACKGROUND: Netherton syndrome (NS) is a severe autosomal recessive ichthyosis. It is characterized by congenital ichthyosiform erythroderma, trichorrhexis invaginata, ichthyosis linearis circumflexa, atopic diathesis, and frequent bacterial infections. The disease is caused by mutations in the SPIN...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3401839/ https://ncbi.nlm.nih.gov/pubmed/22837558 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0019-5154.97660 |
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