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A functional polymorphism in the SPINK5 gene is associated with asthma in a Chinese Han Population
BACKGROUND: Mutation in SPINK5 causes Netherton syndrome, a rare recessive skin disease that is accompanied by severe atopic manifestations including atopic dermatitis, allergic rhinitis, asthma, high serum IgE and hypereosinophilia. Recently, single nucleotide polymorphism (SNP) of the SPINK5 was s...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2709655/ https://ncbi.nlm.nih.gov/pubmed/19534795 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-10-59 |
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