A Case Series of α-Thalassemia Intermedia Due to Compound Heterozygosity for Hb Adana [HBA2: c179G>A (orHBA1); p.Gly60Asp] With Other α-Thalassemias in Malay Families-Reference-Cited by-同舟云学术

A Case Series of α-Thalassemia Intermedia Due to Compound Heterozygosity for Hb Adana [HBA2: c179G>A (orHBA1); p.Gly60Asp] With Other α-Thalassemias in Malay Families

Published:2014-05-14 Issue:4 Volume:38 Page:277-281
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Alauddin Hafiza,Jaapar Noor-Adilah,Azma Raja Z.,Ithnin Azlin,Razak Noor-Farisah A.,Loh C-Khai,Alias Hamidah,Abdul-Latiff Zarina,Othman Ainoon

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2014.916720

Reference24 articles.

1. Haemoglobinopathy Diagnosis

2. Hemoglobin H disease: not necessarily a benign disorder

Cited by 9 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. Hematological Profile of Hb Adana Among High School Students in Northeast Peninsular Malaysia;Cureus;2024-03-31

2. Global Globin Network and adopting genomic variant database requirements for thalassemia;Database;2024

3. Haematologic Profile of Haemoglobin Constant Spring and Its Co-inheritance With Alpha and Beta Thalassaemia Among Form Four Students in Negeri Sembilan;LABORATORY R_T;2022-12-12

4. Clinical and Haematological Parameters of Commonly Reported Non-deletional α-thalassaemia Mutations in Southeast Asia: A Review;Malaysian Journal of Medicine and Health Sciences;2022-09-15

5. A Unique Interaction of IVS-I-1 (G>A) (HBA2: c.95+1G>A) with Hb Adana (HBA2: c.179G>A) Presenting as Transfusion-Dependent α-Thalassemia;Hemoglobin;2018-07-04