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

Clin Chem Lab Med. 2024 Jun 12;62(12):e271-e273. doi: 10.1515/cclm-2024-0452. Print 2024 Nov 26.
No abstract available

Keywords: ATRX gene mutation; HbH disease; capillary electrophoresis.

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Electrophoresis, Capillary*
  • Humans
  • Male
  • Middle Aged
  • Mutation*
  • Nuclear Proteins / genetics
  • X-linked Nuclear Protein* / genetics
  • alpha-Thalassemia* / blood
  • alpha-Thalassemia* / diagnosis
  • alpha-Thalassemia* / genetics

Substances

  • X-linked Nuclear Protein
  • ATRX protein, human
  • Nuclear Proteins