c.49T>C mutation on the α-(1,2)-fucosyltransferase gene responsible for an individual with para-Bombay phenotype-Reference-Cited by-同舟云学术

c.49T>C mutation on the α-(1,2)-fucosyltransferase gene responsible for an individual with para-Bombay phenotype

Published:2018-02-13 Issue:4 Volume:58 Page:1076-1077
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:Transfusion

Author:

Hong Xiaozhen¹,Chen Shu¹,Ma Kairong¹,He Ji¹,Zhu Faming¹

Affiliation:

1. Blood Center of Zhejiang Province; the Key Laboratory of Blood Safety Research, Ministry of Health; and the Zhejiang Provincial Key Laboratory of Blood Safety Research; Hangzhou Zhejiang People's Republic of China.

Funder

Research Foundation of Zhejiang Province

Medical Science Research Foundation of Zhejiang Province

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/trf.14499/fullpdf

Reference4 articles.

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2. BGMUT database of allelic variants of genes encoding human blood group antigens;Patnaik;Transfus Med Hemother,2014

3. Serological characteristic and molecular basis of A2 subgroup in the Chinese population;Ying;Transfus Apher Sci,2013

4. Molecular basis for para-Bombay phenotypes in Chinese persons, including a novel nonfunctional FUT1 allele;Yan;Transfusion,2005

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1. Identification of two novel FUT1 alleles in a Chinese para‐Bombay individual;Transfusion;2022-09-28

2. A novel FUT1 variant allele was identified in a Chinese Para‐Bombay individual;Transfusion;2021-10-24

3. Neonatal testing leading to the identification of Bh (para-Bombay) phenotype in the mother: case report with review of the literature;Immunohematology;2021-06