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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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Pubblicato in:Zhonghua Xue Ye Xue Za Zhi
Natura: Artigo
Lingua:Inglês
Pubblicazione: Editorial office of Chinese Journal of Hematology 2018
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Accesso online: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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