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Article

Global sequencing approach for characterizing the molecular background of hereditary iron disorders.

Clinical chemistry - 1 Dec 2007

Cunat Séverine, Giansily-Blaizot Muriel, Bismuth Michael, Blanc François, Dereure Olivier, Larrey Dominique, Quellec Alain Le, Pouderoux Philippe, Rose Christian, Raingeard Isabelle, Renard Eric, Schved Jean-François, Aguilar-Martinez Patricia

Abstract excerpt

BACKGROUND: New genetic forms of hereditary hemochromatosis (HH) or hereditary hyperferritinemia (HF) have been identified over the last few years, and abnormalities of various genes may interact in a single patient. This study aimed to develop a rapid automated method for sequencing the main genes involved. METHODS: We used a standard 96-well microplate with a single PCR condition in an adaptation of the SCAIP...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 17951290
DOI: 10.1373/clinchem.2007.090605

Genes

HFE
FTL
HAMP
HJV
TFR2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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