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Article

Delayed fetal hemoglobin switching in subjects with KLF1 gene mutation.

Blood cells, molecules & diseases - 15 Jan 2012

Satta Stefania, Perseu Lucia, Maccioni Liliana, Giagu Nicolina, Galanello Renzo

Abstract excerpt

Variations at the KLF1 gene have been associated with a series of human erythroid phenotypes including the In-(Lu) phenotype, hereditary persistence of fetal hemoglobin, congenital dyserythropoietic anemia, borderline HbA(2) and increased red blood cell protoporphyrin. Natural mutations have show...

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Source

Identifiers

PMID: 22093801
DOI: 10.1016/j.bcmd.2011.10.003

Genes

KLF1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Prepared record publication-22093801-2026-09-05.1. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 5 Sept 2026.

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