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A Novel WASP Gene Mutation in a Chinese Boy with Wiskott–Aldrich Syndrome
Wiskott–Aldrich syndrome (WAS) is a rare inherited X-linked recessive immunodeficiency disease characterized by eczema, thrombocytopenia, immune deficiency, and bloody diarrhea and is caused by WASP gene mutations. This study reports a case of WAS with a novel mutation. A newborn Chinese infant was...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Springer India
2014
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4192215/ https://ncbi.nlm.nih.gov/pubmed/25332617 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12288-014-0403-3 |
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