Congenital dyserythropoietic anemia type IV with KLF1 E325K mutation: A new case with dysmorphic male genitalia
- 24 March 2024
- journal article
- letter
- Published by Wiley in Pediatric Blood & Cancer
- Vol. 71 (6) , e30955
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
- Congenital dyserythropoietic anemia type IV in the genetic era: A rare neonatal case report of rapid identification with a review of the literaturePediatric Blood & Cancer, 2023
- The congenital dyserythropoieitic anemias: genetics and pathophysiologyCurrent Opinion in Hematology, 2021
- Congenital Anemia Phenotypes Due to KLF1 MutationsJournal of Pediatric Hematology/Oncology, 2021
- Congenital dyserythropoietic anemia type IV with high fetal hemoglobin caused by heterozygous KLF1 p.Glu325Lys: first report in an Indian infantAnnals of Hematology, 2020
- KLF1 E325K-associated Congenital Dyserythropoietic Anemia Type IV: Insights Into the Variable Clinical SeverityJournal of Pediatric Hematology/Oncology, 2018
- A Case of Congenital Dyserythropoeitic Anemia Type IV Caused by E325K Mutation in Erythroid Transcription Factor KLF1Journal of Pediatric Hematology/Oncology, 2018
- A case of congenital dyserythropoietic anemia type IVClinical Case Reports, 2017
- Erythroid transcription factor EKLF/KLF1 mutation causing congenital dyserythropoietic anemia type IV in a patient of Taiwanese origin: Review of all reported cases and development of a clinical diagnostic paradigmBlood Cells, Molecules, and Diseases, 2013
- A Dominant Mutation in the Gene Encoding the Erythroid Transcription Factor KLF1 Causes a Congenital Dyserythropoietic AnemiaThe American Journal of Human Genetics, 2010
- Congenital dyserythropoietic anaemia with novel intra‐erythroblastic and intra‐erythrocytic inclusionsBritish Journal of Haematology, 1991