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Relative iron deficiency in hereditary spherocytosis

✍ Scribed by Dr. A. Zanella; G. Barosi; A. Berzuini; M. B. Colombo; S. Quaglini; D. Volpes; G. Sirchia


Publisher
John Wiley and Sons
Year
1989
Tongue
English
Weight
445 KB
Volume
31
Category
Article
ISSN
0361-8609

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Spectrin mutations in hereditary ellipto
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## Communicated b~ R. G. H. Cotton Hereditary elliptocytosis (HE), its aggravated form hereditary pyropoikilocytosis (HPP), and hereditary spherocytosis (HS) designate a set of congenital hemolytic syndromes. The responsible mutations lie in several genes encoding proteins of the red cell membrane