Novel mutation in <i>KIF23</i> causing congenital dyserythropoietic anemia type III in patients who underwent allogeneic hematopoietic stem cell transplantation-Reference-Cited by-同舟云学术

Novel mutation in KIF23 causing congenital dyserythropoietic anemia type III in patients who underwent allogeneic hematopoietic stem cell transplantation

Published:2024-03-24 Issue:6 Volume:71 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatric Blood & Cancer

Author:

Fujikawa Tomoko¹,Uemura Suguru¹^ORCID,Hasegawa Daiichiro¹^ORCID,Morisada Naoya²,Nakamura Sayaka¹,Kozaki Aiko¹,Saito Atsuro¹,Kishimoto Kenji¹,Ishida Toshiaki¹,Mori Takeshi¹,Yakushijin Kimikazu³,Katayama Yoshio⁴,Yamashita Daiki⁵,Wakamatsu Manabu⁵,Hamada Motoharu⁵,Muramatsu Hideki⁵,Takahashi Yoshiyuki⁵,Kosaka Yoshiyuki¹

Affiliation:

1. Department of Hematology and Oncology Kobe Children's Hospital Kobe Japan

2. Department of Clinical Genetics Kobe Children's Hospital Kobe Japan

3. Department of Medical Oncology and Hematology Kobe University Hospital Kobe Japan

4. Hematology Kobe University Hospital Kobe Japan

5. Department of Pediatrics Nagoya University Graduate School of Medicine Nagoya Japan

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.30736

Reference12 articles.

1. Congenital dyserythropoietic anemias

2. Congenital dyserythropoietic anemia type III (CDA III) is caused by a mutation in kinesin family member, KIF23

3. RACGAP1 variants in a sporadic case of CDA III implicates the dysfunction of centralspindlin as the basis of the disease

4. Mutations in the <i>RACGAP1</i> gene cause autosomal recessive congenital dyserythropoietic anemia type III

5. Congenital dyserythropoietic anemia types Ib, II, and III: novel variants in the CDIN1 gene and functional study of a novel variant in the KIF23 gene