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Cosmc基因突变与儿童过敏性紫癜易感性的相关性分析
OBJECTIVE: To investigate the presence of Cosmc gene mutation in children with Henoch-Schönlein purpura (HSP) and the association between Cosmc gene mutation and the susceptibility to HSP. METHODS: Eighty-four children who were diagnosed with HSP between March 2014 and December 2015 were selected as...
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| Gepubliceerd in: | Zhongguo Dang Dai Er Ke Za Zhi |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
中国当代儿科杂志编辑部
2016
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7388992/ https://ncbi.nlm.nih.gov/pubmed/27412546 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7499/j.issn.1008-8830.2016.07.011 |
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