Identification and pedigree study of a case with McLeod phenotype caused by XK gene c. 107G>A mutation

[Objective] To identify the phenotypes, antibodies and explore the molecular mechanisms of a patient who carries antibodies to RBC high-frequency antigens and his family members. [Methods] The antibody identification test was performed for the proband by serological methods, and targeted NGS was sub...

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Opis bibliograficzny

Główni autorzy:	ZHANG Yan, WU Yunxiang, WANG Fei, LI Aijing, WANG Hua, LI Minghao, ZHANG Demei, YE Luyi
Format:	Artigo
Język:	Chinês
Wydane:	Institute of Blood Transfusion of Chinese Academy of Medical Sciences 2025-09-01
Seria:	Zhongguo shuxue zazhi
Hasła przedmiotowe:	mcleod phenotype xk gene kell antigen kx antigen
Dostęp online:	https://www.cjbt.cn/thesisDetails#10.13303/j.cjbt.issn.1004-549x.2025.09.021&lang=en
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