Assessment of male CVID patients for mutations in the Btk gene: how many have been misdiagnosed?

The presentation of hypogammaglobulinaemia in young males without a family history of immunodeficiency can pose a diagnostic problem. In the past, the presence of B-cells has suggested a diagnosis of common variable immunodeficiency (CVID), although genotypic analysis has now clarified that individu...

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Bibliografiske detaljer
Main Authors: Weston, S A, Prasad, M L, Mullighan, C G, Chapel, H, Benson, E M
Format: Artigo
Sprog:English
Udgivet: Blackwell Science Inc 2001
Fag:
Immunodeficiency
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1906085/
https://ncbi.nlm.nih.gov/pubmed/11472409
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1046/j.1365-2249.2001.01556.x
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Internet

https://ncbi.nlm.nih.gov/pmc/articles/PMC1906085/
https://ncbi.nlm.nih.gov/pubmed/11472409
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1046/j.1365-2249.2001.01556.x

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