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Mutational Characteristics of Causative Genes in Chinese Hereditary Spherocytosis Patients: a Report on Fourteen Cases and a Review of the Literature
Background: Hereditary spherocytosis (HS), characterized by the presence of spherocytic red cells in peripheral blood, hemolysis, splenomegaly, jaundice, and gallstones, is a common form of inherited hemolytic anemia (HA). To date, five causative genes associated with HS have been identified, includ...
Autores principales: | Wang, Dong, Song, Li, Shen, Li, Zhang, Kaihui, Lv, Yuqiang, Gao, Min, Ma, Jian, Wan, Ya, Gai, Zhongtao, Liu, Yi |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8322660/ https://www.ncbi.nlm.nih.gov/pubmed/34335240 http://dx.doi.org/10.3389/fphar.2021.644352 |
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