A 6-Year Follow-up of a Chinese Child with Homozygous β <sup>0</sup> -Thalaasemia and a Heterozygous <i>KLF1</i> Mutation-Reference-Cited by-同舟云学术

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A 6-Year Follow-up of a Chinese Child with Homozygous β ⁰ -Thalaasemia and a Heterozygous KLF1 Mutation

Published:2024-01-02 Issue:1 Volume:48 Page:60-62
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Wu Shao-Min¹,Li Chan¹,Huang Su-Ran¹,Jiang Fan²,Li Dong-Zhi²

Affiliation:

1. Prenatal Diagnosis Center, The Tenth Affiliated Hospital, Southern Medical University (Dongguan People’s Hospital), Dongguan, People’s Republic of China

2. Prenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, Guangdong Province, People’s Republic of China

Funder

Provincial Department of Science and Technology Agency of Guangdong

Guangdong Natural Science Foundation

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2024.2310804

Reference13 articles.

1. β-Thalassemias

2. A Melting Curve Analysis–Based PCR Assay for One-Step Genotyping of β-Thalassemia Mutations

3. 4 Pathophysiology of thalassaemia

4. Pathophysiology and Clinical Manifestations of the -Thalassemias

5. The prevalence and spectrum of and thalassaemia in Guangdong Province: implications for the future health burden and population screening

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