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遗传性球形红细胞增多症红细胞膜蛋白基因突变的临床特征研究
OBJECTIVE: To investigate the relationship between the erythrocyte membrane protein gene mutations and the clinical severity of hereditary spherocytosis (HS). METHODS: Targeted sequencings were performed on 25 HS patients, correlation between HS mutations and patients' clinical characteristics...
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| Publicado no: | Zhonghua Xue Ye Xue Za Zhi |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Editorial office of Chinese Journal of Hematology
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7342345/ https://ncbi.nlm.nih.gov/pubmed/30486587 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3760/cma.j.issn.0253-2727.2018.11.008 |
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