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Le profil clinique et immunologique de 15 patients Marocains atteints de syndrome hyper IgM
Hyper IgM syndrome is a well known genetic (primary) immunodeficiency disorder which was first described in 1961. It is caused by B lymphocyte deficiency characterized by normal or elevated serum IgM levels and low or zero levels of IgG, IgA, IgE resulting from isotype-switching deficiency. Clinical...
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| Pubblicato in: | Pan Afr Med J |
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| Autori principali: | , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
The African Field Epidemiology Network
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5491719/ https://ncbi.nlm.nih.gov/pubmed/28690727 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11604/pamj.2017.26.212.10081 |
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