Dominantly inherited thalassaemia intermedia caused by a new single nucleotide deletion in exon 2 of the globin gene: Hb morgantown ( 91 CTG>CG)
Author:
Publisher
BMJ
Subject
General Medicine,Pathology and Forensic Medicine
Cited by 11 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Dominantly Inherited β-Thalassemia Caused by a Single Nucleotide Deletion in Exon 3 of the β-Globin Gene: Hb Xiangyang (HBB: c.393delT);Hemoglobin;2022-06-10
2. Compound Heterozygosity for a Novel Mutation Codon 104 (–A) (HBB: c.313delA) and Codons 41/42 (–CTTT) (HBB: c.126_129delCTTT) Leading to β-Thalassemia Major in a Chinese Family;Hemoglobin;2020-11-01
3. Two novel unstable hemoglobin variants due to in-frame deletions of key amino acids in the β-globin chain;European Journal of Haematology;2018-03-01
4. Double heterozygosity for hemoglobin C and beta-thalassemia dominant: A rare case of thalassemia intermedia;Hematology Reports;2018-01-03
5. Diverse hematological phenotypes of β-thalassemia carriers;Annals of the New York Academy of Sciences;2016-03
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