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Article

Reliability of DHPLC in mutational screening of beta-globin (HBB) alleles.

Human mutation - 1 Mar 2002

Colosimo Alessia, Guida Valentina, De Luca Alessandro, Cappabianca Maria Pia, Bianco Ida, Palka Giandomenico, Dallapiccola Bruno

Abstract excerpt

The inherited disorders of hemoglobin represent the most common Mendelian disease worldwide, with a higher prevalence among Mediterraneans, Asians, Africans, and Indians. Altered beta-globin sequences, causing either hemoglobinopathies or beta-thalassemia syndromes, are due to more than 200 diffe...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 11857746
DOI: 10.1002/humu.10046

Genes

HBB

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-11857746-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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