Hb Prato [α31(B12)Arg→Ser (α2)] and α‐Thalassemia in a Taiwanese-Reference-Cited by-同舟云学术

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Hb Prato [α31(B12)Arg→Ser (α2)] and α‐Thalassemia in a Taiwanese

Published:2003-01 Issue:1 Volume:27 Page:45-47
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Shih Mu‐Chin,Peng Ching‐Tien,Chang Jan‐Yi,Liu Su‐Ching,Kuo Pao‐Lin,Chang Jan‐Gowth

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.1081/HEM-120018436

Reference6 articles.

1. A new abnormal human hemoglobin: Hb prato (α231 (B12) Arg→Ser β2)

2. Hb Prato α31(B12)Arg→ser] in a Calabrian Family

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

4. Rapid molecular characterization of Hb H disease in Chinese by polymerase chain reaction

5. Hb MANITOBA IN A TAIWANESE FAMILY: A C → A SUBSTITUTION AT CODON 102 OF THE α2-GLOBIN GENE

Cited by 3 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. α-Thalassemia Intermedia Results from Interactions of Unstable Hb Prato [α31(B12)Arg→Ser (HBA1 or HBA2 c.96G>T or C)] with the α-Thalassemia-1 [– –SEA (Southeast Asian)] Deletion in Thailand;Hemoglobin;2020-07-03

2. Hb Cervantes, Hb Marañón, Hb La Mancha and Hb Goya: Description of 4 new haemoglobinopathies;Clinical Biochemistry;2015-07

3. Analysis of human α globin gene mutations that impair binding to the α hemoglobin stabilizing protein;Blood;2009-06-04

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