A Novel Case of Hb Phnom Penh: Codons 117/118 (+ATC) as a Cause of α+-Thalassemia
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269.2012.665402
Reference10 articles.
1. Genetic and Clinical Features of Hemoglobin H Disease in Chinese Patients
2. Locus assignment of human a globin mutations by selective amplification and direct sequencing
3. Hb Aghia Sophia [α62(E11)Val→0 (α1)], an “In-Frame” Deletion Causing α-Thalassemia
4. A Rare 33 bp In‐Frame Deletion (α63–74 or α64–74 or α65–75) in the α1‐Globin Gene Causing α+‐Thalassemia: A Second Observation
5. Further Identification of The Hyperunstable α-Globin Chain Variant Hb Heraklion [codons 36/37 (–CCC); Pro→0 (α1)] in Greek Cases With Co-Inherited α+-Thalassemia Mutations
Cited by 1 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. Association of Hb Thailand [α56(E5)Lys→Thr] and Hb Phnom Penh [α117(GH5)-Ile-α118(H1)] withα0-Thalassemia: Molecular and Hematological Features and Differential Diagnosis;Hemoglobin;2012-12-07
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