Mutations of the Igβ gene cause agammaglobulinemia in man

Agammaglobulinemia is a rare primary immunodeficiency characterized by an early block of B cell development in the bone marrow, resulting in the absence of peripheral B cells and low/absent immunoglobulin serum levels. So far, mutations in Btk, μ heavy chain, surrogate light chain, Igα, and B cell l...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Ferrari, Simona, Lougaris, Vassilios, Caraffi, Stefano, Zuntini, Roberta, Yang, Jianying, Soresina, Annarosa, Meini, Antonella, Cazzola, Giantonio, Rossi, Cesare, Reth, Michael, Plebani, Alessandro
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: The Rockefeller University Press 2007
Aiheet:
Brief Definitive Reports
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2118692/
https://ncbi.nlm.nih.gov/pubmed/17709424
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1084/jem.20070264
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