Molecular and cellular characterization of congenital dyserythropoietic anaemia type 1

Congenital dyserythropoietic anaemia type 1 (CDA I) is an autosomal recessive disorder of erythropoiesis characterized by a clinical picture of anaemia secondary to ineffective erythropoiesis, haemolysis and striking morphology of erythroid precursors (inteternuclear chromatin bridges, spongy hetero...

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Bibliographic Details
Main Author: Ahmed, Momin
Published: Open University 2009
Subjects:
Online Access:http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.499453