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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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2018
Materias:
论著
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

Internet

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

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