Evolution of acquired haemoglobin H disease monitored by capillary electrophoresis: a case of a myelofibrotic patient with a novel ATRX mutation
M Rosetti, G Poletti, R Catapano… - Clinical Chemistry and …, 2024 - degruyter.com
Haemoglobin H (Hb H) disease is a severe non-fatal congenital form of α-thalassemia
syndrome particularly prevalent in the Middle East resulting from the presence of only one …
syndrome particularly prevalent in the Middle East resulting from the presence of only one …