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Screening of functional and positional candidate genes in families with common variable immunodeficiency

BACKGROUND: Common variable immunodeficiency (CVID) comprises a heterogeneous group of primary antibody deficiencies with complex clinical and immunological phenotypes. The recent discovery that some CVID patients show monogenic defects in the genes encoding ICOS, TACI or CD19 prompted us to investi...

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Autores principales: Salzer, Ulrich, Neumann, Carla, Thiel, Jens, Woellner, Cristina, Pan-Hammarström, Qiang, Lougaris, Vassilis, Hagena, Tina, Jung, Johannes, Birmelin, Jennifer, Du, Likun, Metin, Ayse, Webster, David A, Plebani, Alessandro, Moschese, Viviana, Hammarström, Lennart, Schäffer, Alejandro A, Grimbacher, Bodo
Formato: Artigo
Lenguaje:Inglês
Publicado: BioMed Central 2008
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC2268914/
https://ncbi.nlm.nih.gov/pubmed/18254984
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2172-9-3
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