Point mutations which should not be overlooked in Hb H disease
Author:
Publisher
Informa UK Limited
Subject
Hematology
Link
http://www.tandfonline.com/doi/pdf/10.1586/17474086.2016.1107470
Reference42 articles.
1. Two different molecular organizations account for the single alpha-globin gene of the alpha-thalassemia-2 genotype.
2. A Gradient of Sequence Divergence in the Human Adult α-Globin Duplication Units
3. The chromosomal arrangement of human α-like globin genes: Sequence homology and α-globin gene deletions
4. A large deletion in the human -globin cluster caused by a replication error is associated with an unexpectedly mild phenotype
Cited by 4 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. Genotype–phenotype correlation in patients with deletional and nondeletional mutations of Hb H disease in Southwest of Iran;Scientific Reports;2022-03-22
2. Genotype-phenotype correlation of HbH disease in northern Iraq;BMC Medical Genetics;2020-10-15
3. A Nested Asymmetric PCR Melting Curve Assay for One-Step Genotyping of Nondeletional α-Thalassemia Mutations;The Journal of Molecular Diagnostics;2020-06
4. α-Globin Genotypes Associated with Hb H Disease: A Report from Oman and a Review of the Literature from the Eastern Mediterranean Region;Hemoglobin;2020-01-02
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