A Case of Hereditary Spherocytosis Caused by a Novel Homozygous Mutation in the SPTB Gene Misdiagnosed as β-Thalassemia Intermedia Due to a KLF1 Gene Mutation

Kun Yang,Quan Ren,Yi Wu,Ya-Li Zhou,Xiao-Lin Yin

A Case of Hereditary Spherocytosis Caused by a Novel Homozygous Mutation in the SPTB Gene Misdiagnosed as β-Thalassemia Intermedia Due to a KLF1 Gene Mutation

2019

Kun Yang
Quan Ren
Yi Wu
Ya-Li Zhou
Xiao-Lin Yin

AbstractWe report a rare case of hereditary spherocytosis (HS) and hereditary persistence of fetal hemoglobin (Hb) (HPFH) complicated with a β-thalassemia (β-thal) trait and a Kruppel-like factor 1...

Keywords:

Molecular biology
Biology
Genetics
KLF1
Gene
Thalassemia intermedia
Mutation
Hereditary spherocytosis
Thalassemia
gene mutation
β thalassemia intermedia
Hereditary persistence of fetal hemoglobin

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