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Article

Evaluation of HPFH and δβ-thalassemia mutations in a Brazilian group with high Hb F levels.

Genetics and molecular research : GMR - 21 Dec 2011

Carrocini G C S, Ondei L S, Zamaro P J A, Bonini-Domingos C R

Abstract excerpt

Fetal hemoglobin (Hb F) is characteristic of the fetal development period. However, in some genetic conditions, such as hereditary persistence of fetal hemoglobin (HPFH) and delta-beta thalassemia (δβ-thalassemia), Hb F continues to be produced in adulthood. We evaluated the frequency of two mutations of HPFH, HPFH-1 and HPFH-2 African, and two mutations in δβ-thalassemia, Sicilian and Spanish, in a...

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PMID: 22194178
DOI: 10.4238/2011.December.21.3

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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