A novel variant of SLC4A1 for hereditary spherocytosis in a Chinese family: a case report and systematic review

BACKGROUND: The incidence of hereditary spherocytosis (HS) is approximately 1:2000 in the western population, while it is much lower in the Chinese population. It is difficult to make a definite diagnosis due to the variable genotypic features and the lack of well-documented evidence for HS patients...

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Detalles Bibliográficos
Autores principales: Li, Jie, Wang, Xiaozi, Zheng, Na, Wang, Xiaoning, Liu, Yan, Xue, Liying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9719243/
https://www.ncbi.nlm.nih.gov/pubmed/36463227
http://dx.doi.org/10.1186/s12920-022-01399-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9719243/
https://www.ncbi.nlm.nih.gov/pubmed/36463227
http://dx.doi.org/10.1186/s12920-022-01399-2

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