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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Detalles Bibliográficos
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: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2268914/
https://www.ncbi.nlm.nih.gov/pubmed/18254984
http://dx.doi.org/10.1186/1471-2172-9-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2268914/
https://www.ncbi.nlm.nih.gov/pubmed/18254984
http://dx.doi.org/10.1186/1471-2172-9-3

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