A novel nonsense mutation in RHAG gene responsible for Rh null phenotype in a Chinese individual-Reference-Cited by-同舟云学术

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A novel nonsense mutation in RHAG gene responsible for Rh null phenotype in a Chinese individual

Published:2017-04 Issue:2 Volume:56 Page:220-222
ISSN:1473-0502
Container-title:Transfusion and Apheresis Science
language:en
Short-container-title:Transfusion and Apheresis Science

Author:

Hou Li,Yan Qi-dong,Tian Li

Publisher

Elsevier BV

Subject

Hematology

Reference15 articles.

1. Rh-deficiency syndrome;Cartron;Lancet,2001

2. The Rh blood group system: a review;Avent;Blood,2000

3. RH blood group system and molecular basis of Rh-deficiency;Cartron;Baillieres Best Pract Res Clin Haematol,1999

4. Two-step approaches for RHD gene analysis of RhD negatives and variants and the discovery of a new allele;Lu;Chin J Blood Transfusion,2011

5. A family study of the Chinese Rhnull individual of the regulator type: a novel single missense mutation identified in RHAG gene;Tian;Transfusion,2011

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. A novel frameshift mutation in RHAG leads to Rh_null phenotype in a Chinese individual;Transfusion;2024-04-02

2. A novel mutation in RHAG causing Rh null phenotype in Colombia;Transfusion;2021-07-26

3. Extensive clinical, serologic and molecular studies lead to the first reported Rh mod phenotype in Argentina;Transfusion;2020-05-06

4. A novel nucleotide deletion in RHAG allele identified in a Chinese Rhnull individual;Transfusion;2017-12-21

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