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Development of lentiviral gene therapy for Wiskott Aldrich syndrome
BACKGROUND: Wiskott Aldrich Syndrome (WAS) is a rare X-linked primary immunodeficiency. This complex disease is characterised by micro-thrombocytopenia, recurrent infections, eczema and is associated with a high incidence of auto-immunity and of lymphoid malignancies. WAS is attracting growing atten...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Informa Healthcare
2008
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2789278/ https://ncbi.nlm.nih.gov/pubmed/18194074 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1517/14712598.8.2.181 |
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