Cargando…
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...
Formato: | Online Artículo Texto |
---|---|
Lenguaje: | English |
Publicado: |
Editorial office of Chinese Journal of Hematology
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342345/ https://www.ncbi.nlm.nih.gov/pubmed/30486587 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2018.11.008 |
Ejemplares similares
-
遗传性球形红细胞增多症ANK1基因新突变一例
Publicado: (2017) -
遗传性球形红细胞增多症骨髓红系造血代偿特征
Publicado: (2022) -
遗传性球形红细胞增多症SPTB新突变一例
Publicado: (2019) -
EMA结合试验检测的红细胞膜带3蛋白缺失程度与遗传性球形红细胞增多症临床表现型的关系
Publicado: (2017) -
37例遗传性球形细胞增多症基因突变特征分析
Publicado: (2018)