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Congenital Nonspherocytic Hemolytic Anemia Caused by Krüppel-Like Factor 1 Gene Variants: Another Case Report.

Hemoglobin - 1 Jan 2000

Jiang Hua, Jiang Fan, Li Jian, Tang Fang, Li Dong-Zhi

Abstract excerpt

In this study, we report on a compound heterozygote for variants in the key erythroid transcription factor Krüppel-like factor 1 (KLF1) gene in a patient who presented with severe, transfusion-dependent hemolytic anemia. The red cells were normochromic and normocytic, and resembled those seen in patients with congenital nonspherocytic hemolytic anemia (CNSHA). Next generation sequencing (NGS) revealed that the...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 31645145
DOI: 10.1080/03630269.2019.1680384

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

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