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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Detalhes bibliográficos
Main Authors: 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
Idioma:Inglês
Publicado em: BioMed Central 2008
Assuntos:
Research Article
Acesso em linha: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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