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Article

Multiplex analysis of the most common mutations related to hereditary haemochromatosis: two methods combining specific amplification with capillary electrophoresis.

European journal of haematology - 1 Feb 2004

Gómez-Llorente Carolina, Antúnez Adelaida, Blanco Sonia, Suarez Antonio, Gómez-Capilla Jose Antonio, Farez-Vidal M Esther

Abstract excerpt

We present the first application of a multiplex multicolour assay for the simultaneous detection of three of the most frequent mutations related to hereditary haemochromatosis (C282Y, H63D and S65C), using fluorescent detection and capillary electrophoresis. We describe two methods: the first is...

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Source

Identifiers

PMID: 14962249
DOI: 10.1046/j.0902-4441.2003.00186.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-14962249-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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Multiplex analysis of the most common mutations related to hereditary haemochromatosis: two methods combining specific amplification with capillary electrophoresis.PMID 14962249Read ↗

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Integration of combined heteroduplex/restriction fragment length polymorphism analysis on an electrophoresis microchip for the detection of hereditary haemochromatosis.Semantic proximity Read ↗

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