# A Very Rare Congenital Dyserythropoietic Anemia Variant—Type IV in a Patient With a Novel Mutation in the KLF1 Gene: A Case Report and Review of the Literature

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/a-very-rare-congenital-dyserythropoietic-anemia-variant-type-iv-in-a-patient/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Tugba Belgemen‐Ozer,Orhan Görükmez |
| Citations | 16 |
| DOI | 10.1097/mph.0000000000001727 |
| Fields | Medicine |
| Open Access | false |
| OA Status | closed |
| OpenAlex ID | https://openalex.org/W3005271733 |
| PMID | 32032242 |
| Type | article |
| Year | 2020 |

## Paper authors

- [Orhan Görükmez](https://scholariq.org/researchers/orhan-gorukmez/)

## Paper journal

- [Journal of Pediatric Hematology/Oncology](https://scholariq.org/journals/journal-of-pediatric-hematology-oncology/)

## Paper primary topic

- [Erythrocyte Function and Pathophysiology](https://scholariq.org/topics/erythrocyte-function-and-pathophysiology/)

## Paper topics

- [Erythrocyte Function and Pathophysiology](https://scholariq.org/topics/erythrocyte-function-and-pathophysiology/)
- [Blood properties and coagulation](https://scholariq.org/topics/blood-properties-and-coagulation/)
- [Hemoglobinopathies and Related Disorders](https://scholariq.org/topics/hemoglobinopathies-and-related-disorders/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.