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

Authors :: Rosetti M
Poletti G
Catapano R
Trombetti S
Grosso M
Maoggi S
Ivaldi G
Massari E
Monti M
Olivieri M
Polli V
Clementoni A
Fasano T
Source :: Clinical chemistry and laboratory medicine [Clin Chem Lab Med] 2024 Jun 12; Vol. 62 (12), pp. e271-e273. Date of Electronic Publication: 2024 Jun 12 (Print Publication: 2024).
Publication Year :: 2024

Subjects :: Humans
Male
Nuclear Proteins genetics
Middle Aged
X-linked Nuclear Protein genetics
Mutation
Electrophoresis, Capillary
alpha-Thalassemia genetics
alpha-Thalassemia blood
alpha-Thalassemia diagnosis

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