First Detection of a Splice Siteβ-Thalassemia Mutation, IVS-I-6 (T > C) (HBB: c.92 + 6T > C) in a Chinese Family
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269.2015.1027826
Reference11 articles.
1. The Thalassaemia Syndromes
2. A novel β-globin gene deletion (codons 89–93) in a Chinese family
3. First detection of the codons 41–43 (−CTTTG,+A) β-thalassemia mutation in a Chinese patient
4. Prenatal diagnosis of β-thalassemia in Guangxi Zhuang Autonomous Region, China
5. Severity of β-thalassemia due to genotypes involving the IVS-I-6 (T→C) mutation
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1. A survey of intracranial blood flow velocity in thalassemia intermedia in Khuzestan Province, Iran;Iranian Journal of Pediatric Hematology & Oncology;2023-01-03
2. A Novel β-Thalassemia Mutation [IVS-I-6 (T>G), HBB: c.92+6T>G] in a Chinese Family;Hemoglobin;2020-01-02
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