Evolution of acquired haemoglobin H disease monitored by capillary electrophoresis: a case of a myelofibrotic patient with a novel <i>ATRX</i> mutation-Reference-Cited by-同舟云学术

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

Published:2024-06-12 Issue: Volume: Page:
ISSN:1434-6621
Container-title:Clinical Chemistry and Laboratory Medicine (CCLM)
language:en
Short-container-title:

Author:

Rosetti Marco¹^ORCID,Poletti Giovanni¹,Catapano Rosa²,Trombetti Silvia³,Grosso Michela²³,Maoggi Sauro⁴,Ivaldi Giovanni⁵,Massari Evita¹,Monti Marta¹,Olivieri Melania¹,Polli Valentina¹,Clementoni Alice¹,Fasano Tommaso¹

Affiliation:

1. Clinical Pathology Unit, Hub Laboratory , 390233 AUSL della Romagna , Cesena , Italy

2. Ceinge-Biotecnologie Avanzate “Franco Salvatore” , Naples , Italy

3. Department of Molecular Medicine and Medical Biotechnology , 9307 University of Naples Federico II , Naples , Italy

4. Sebia Italia srl , Bagno a Ripoli, Florence , Italy

5. Formerly, Laboratorio Genetica Umana , Ospedali Galliera , Genova , Italy

Publisher

Walter de Gruyter GmbH

Link

https://www.degruyter.com/document/doi/10.1515/cclm-2024-0452/pdf

Reference9 articles.

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2. Forget, BG. De novo and acquired forms of alpha thalassemia. Curr Hematol Rep 2006;5:11–4.

3. Ratnakumar, K, Duarte, LF, LeRoy, G, Hasson, D, Smeets, D, Vardabasso, C, et al.. ATRX-mediated chromatin association of histone variant macroH2A1 regulates α-globin expression. Genes Dev 2012;26:433–8. https://doi.org/10.1101/gad.179416.111.

4. Steensma, DP, Gibbons, RJ, Higgs, DR. Acquired alpha-thalassemia in association with myelodysplastic syndrome and other hematologic malignancies. Blood 2005;105:443–52. https://doi.org/10.1182/blood-2004-07-2792.

5. Jones, JA, Broszeit, HK, LeCrone, CN, Detter, JC. An improved method for detection of red cell hemoglobin H inclusions. Am J Med Technol 1981;47:94–6.