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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Detalhes bibliográficos
Publicado no: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 em: Frontiers Media S.A. 2021
Assuntos:
Genetics
Acesso em linha: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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