Compound Heterozygosity for KLF1 Mutations Causing Hemolytic Anemia in Children: A Case Report and Literature Review

BACKGROUND: Anemia is one of the most common diseases affecting children worldwide. Hereditary forms of anemia due to gene mutations are difficult to diagnose because they only rely on clinical manifestations. In regions with high prevalence of thalassemia such as southern China, pediatric patients...

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Detalles Bibliográficos
Autores principales: Xu, Linlin, Zhu, Dina, Zhang, Yanxia, Liang, Guanxia, Liang, Min, Wei, Xiaofeng, Feng, Xiaoqing, Wu, Xuedong, Shang, Xuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267787/
https://www.ncbi.nlm.nih.gov/pubmed/34249106
http://dx.doi.org/10.3389/fgene.2021.691461

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267787/
https://www.ncbi.nlm.nih.gov/pubmed/34249106
http://dx.doi.org/10.3389/fgene.2021.691461

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