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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Publicado en:Front Genet
Main Authors: Xu, Linlin, Zhu, Dina, Zhang, Yanxia, Liang, Guanxia, Liang, Min, Wei, Xiaofeng, Feng, Xiaoqing, Wu, Xuedong, Shang, Xuan
Formato: Artigo
Idioma:Inglês
Publicado: Frontiers Media S.A. 2021
Assuntos:
Genetics
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC8267787/
https://ncbi.nlm.nih.gov/pubmed/34249106
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2021.691461
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