Recapitulation of erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalities
The investigation of inherited disorders of erythropoiesis has elucidated many of the principles underlying the production of normal red blood cells and how this is perturbed in human disease. Congenital Dyserythropoietic Anaemia type 1 (CDA-I) is a rare form of anaemia caused by mutations in two ge...
Main Authors: | Scott, C, Downes, DJ, Brown, J, Beagrie, R, Olijnik, AA, Gosden, M, Schwessinger, R, Fisher, C, Rose, A, Ferguson, D, Johnson, E, Hill, Q, Okoli, S, Renella, R, Ryan, K, Brand, M, Hughes, J, Roy, N, Higgs, D, Babbs, C, Buckle, V |
---|---|
Format: | Journal article |
Language: | English |
Published: |
Ferrata Storti Foundation
2020
|
Similar Items
-
Functional impairment of erythropoiesis in Congenital Dyserythropoietic Anaemia type I arises at the progenitor level
by: Scott, C, et al.
Published: (2022) -
The pathogenesis, diagnosis and management of congenital dyserythropoietic anaemia type I
by: Roy, N, et al.
Published: (2019) -
A Transgenic Mouse Model for Congenital Dyserythropoietic Anemia Type I
by: Renella, R, et al.
Published: (2008) -
Evidence of genetic heterogeneity in congenital dyserythropoietic anaemia type I.
by: Ahmed, MR, et al.
Published: (2006) -
Congenital dyserythropoietic anemias
by: Renella, R, et al.
Published: (2011)