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Clinical and mutational features of Vietnamese children with X-linked agammaglobulinemia
BACKGROUND: X-linked agammaglobulinemia (XLA) is a primary immune deficiency characterized by recurrent bacterial infections and profoundly depressed serum immunoglobulin levels and circulating mature B cells. It is caused by mutations of the Bruton tyrosine kinase (BTK) gene and is the most common...
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| Hlavní autoři: | , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2014
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4054903/ https://ncbi.nlm.nih.gov/pubmed/24885015 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2431-14-129 |
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