Hb Lansing (HBA2: c.264C > G) and a NewβPromoter Transversion [−52 (G > T)]: An Attempt to Define the Phenotype of Two Mutations Found in the Omani Population-Reference-Cited by-同舟云学术

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Hb Lansing (HBA2: c.264C > G) and a NewβPromoter Transversion [−52 (G > T)]: An Attempt to Define the Phenotype of Two Mutations Found in the Omani Population

Published:2015-03-04 Issue:2 Volume:39 Page:111-114
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Hassan Suha M.,Harteveld Cornelis L.,Bakker Engbert,Giordano Piero C.

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2015.1016615

Reference24 articles.

1. Unstable and Thalassemic α Chain Hemoglobin Variants: A Cause of Hb H Disease and Thalassemia Intermedia

2. Characterization of hemoglobin bassett (?94Asp?Ala), a variant with very low oxygen affinity

3. Evaluating five dedicated automatic devices for haemoglobinopathy diagnostics in multi-ethnic populations

4. Rapid detection of α-thalassaemia deletions and α-globin gene triplication by multiplex polymerase chain reactions

5. Molecular spectrum of ?-thalassemia in the Iranian population of Hormozgan: Three novel point mutation defects

Cited by 2 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. Persistent Hypoxemia in an Asymptomatic 4-year-old Boy;Pediatrics in Review;2023-05-01

2. Borderline HbA2 levels: Dilemma in diagnosis of beta-thalassemia carriers;Mutation Research/Reviews in Mutation Research;2021-07

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