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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Detalles Bibliográficos
Autores principales: Liu, Qiji, Xia, Yu, Zhang, Wenjing, Li, Jisheng, Wang, Pin, Li, Huaichen, Wei, Chunhua, Gong, Yaoqin
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2709655/
https://www.ncbi.nlm.nih.gov/pubmed/19534795
http://dx.doi.org/10.1186/1471-2350-10-59

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2709655/
https://www.ncbi.nlm.nih.gov/pubmed/19534795
http://dx.doi.org/10.1186/1471-2350-10-59

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