Mutational spectrum in congenital dyserythropoietic anemia type II: Identification of 19 novel variants in SEC23B gene
Author:
Publisher
Wiley
Subject
Hematology
Reference18 articles.
1. Hereditary erythroblastic multinuclearity associated with a positive acidified-serum test: A typical congenital dyserythropoietic anemia;Crookston;Br J Haematol,1969
2. Congenital dyserythropoietic anemias;Marks;Am J Hematol,1996
3. Congenital dyserythropoietic anemia type II: Molecular basis and clinical aspects;Iolascon;Haematologica,1996
4. Close to unraveling the secrets of congenital dyserythropoietic anemia types I and II;Iolascon;Haematologica,2009
5. The morphological diagnosis of congenital dyserythropoietic anemia: Results of a quantitative analysis of peripheral blood and bone marrow cells;Heimpel;Haematologica,2010
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1. Identification of a novel splice variant in SEC23B gene in a patient with concomitant presence of congenital dyserythropoietic anemia II and Gilbert’s syndrome;Hematology;2024-04-24
2. The COPII subunit CsSEC23 mediates fruit glossiness in cucumber;The Plant Journal;2023-07-26
3. Development of High-Resolution Melting Curve Analysis for rapid detection of SEC23B gene mutation causing Congenital Dyserythropoietic Anemia type II in Indian population;Italian Journal of Pediatrics;2023-07-16
4. New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II;International Journal of Molecular Sciences;2023-06-09
5. Compound heterozygosity for two novel mutations of the SEC23B gene in congenital dyserythropoietic anemia type II;International Journal of Hematology;2021-04-29
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