Severe neonatal haemolytic anaemia caused by compound heterozygous KLF1 mutations: report of four families and literature review-Reference-Cited by-同舟云学术

Severe neonatal haemolytic anaemia caused by compound heterozygous KLF1 mutations: report of four families and literature review

Published:2021-07-05 Issue:3 Volume:194 Page:626-634
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br. J. Haematol.

Author:

Tangsricharoen Tanu¹,Natesirinilkul Rungrote¹,Phusua Arunee¹,Fanhchaksai Kanda¹,Ittiwut Chupong²³,Chetruengchai Wanna²³,Juntharaniyom Monthana⁴,Charoenkwan Pimlak¹^ORCID,Viprakasit Vip⁵,Phokaew Chureerat²³,Shotelersuk Vorasuk²³

Affiliation:

1. Department of Pediatrics Division of Hematology and Oncology Faculty of Medicine Chiang Mai University Chiang MaiThailand

2. Department of Pediatrics Center of Excellence for Medical Genomics Medical Genomics Cluster Faculty of Medicine Chulalongkorn University BangkokThailand

3. Excellence Center for Genomics and Precision Medicine King Chulalongkorn Memorial Hospital The Thai Red Cross Society BangkokThailand

4. Department of Pediatrics Division of Hematology and Oncology Khon Kaen Regional Hospital Khon KaenThailand

5. Department of Pediatrics Division of Hematology and Oncology Faculty of Medicine Siriraj Hospital Mahidol University Bangkok Thailand

Funder

Faculty of Medicine, Chiang Mai University

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjh.17616

Reference40 articles.