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...

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Detalles Bibliográficos
Autores principales: Wang, Dong, Song, Li, Shen, Li, Zhang, Kaihui, Lv, Yuqiang, Gao, Min, Ma, Jian, Wan, Ya, Gai, Zhongtao, Liu, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Pharmacology
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

Internet

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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