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Evolution of acquired haemoglobin H disease monitored by capillary electrophoresis: a case of a myelofibrotic patient with a novel ATRX mutation.

Clinical chemistry and laboratory medicine - 26 Nov 2024

Rosetti Marco, Poletti Giovanni, Catapano Rosa, Trombetti Silvia, Grosso Michela, Maoggi Sauro, Ivaldi Giovanni, Massari Evita, Monti Marta, Olivieri Melania, Polli Valentina, Clementoni Alice, Fasano Tommaso

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Share to alpha-Thalassemia
Share to Electrophoresis, Capillary
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 38860964
DOI: 10.1515/cclm-2024-0452

Genes

ATRX

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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Evolution of acquired haemoglobin H disease monitored by capillary electrophoresis: a case of a myelofibrotic patient with a novel ATRX mutation.PMID 38860964Read ↗

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