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...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Pubblicato in:Front Genet
Autori principali: Xu, Linlin, Zhu, Dina, Zhang, Yanxia, Liang, Guanxia, Liang, Min, Wei, Xiaofeng, Feng, Xiaoqing, Wu, Xuedong, Shang, Xuan
Natura: Artigo
Lingua:Inglês
Pubblicazione: Frontiers Media S.A. 2021
Soggetti:
Genetics
Accesso online: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
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !

Documenti analoghi