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Autor:
Artor, Niccoli Asabella, Corinna, Altini, Anna G, Nappi, Valentina, Lavelli, Cristina, Ferrari, Andrea, Marzullo, Alessandra, Loiodice, Giuseppe, Rubini
Publikováno v:
Hellenic journal of nuclear medicine. 22(1)
Sickle cell disease (SCD) is the best known haemoglobinopathy, caused by a mutation substituting valina for glutamic acid at position 6 of the beta-globin chain of adult hemoglobin A, resulting in hemoglobin S (HbS). The homozygous HbS disease (HbSS)