What question did this study set out to answer?

The study aims to identify and describe a novel nonsense variant within the ABO*B.01 allele.

April 10, 2026

Identification of a novel nonsense variant ( c.184C>T ) in ABO*B.01 allele

Key Points

The study aims to identify and describe a novel nonsense variant within the ABO*B.01 allele.
Data collected from NCBI GenBank
Reference number provided for data access
Identification of variant c.184C>T
Novel allele variation reported
Data made publicly available for further analysis

Abstract

The authors have disclosed no conflicts of interest. The data that support the findings of this study are openly available in NCBI GenBank at https://www.ncbi.nlm.nih.gov/genbank/, reference number PX627881.

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Authors

Xiaoyun Bu

Wei Zhang

Feng Shao

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Transfusion

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Institutions

Ningxia University

Ningxia Seismological Bureau

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Building similarity graph...

Analyzing shared references across papers

Identification of a novel nonsense variant ( c.184C>T ) in ABO*B.01 allele

Key Points

Abstract

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Connected Papers

Discussion

Authors

Journals

Actions

Institutions

References and Citations

Citation Network

Connected Papers

Discussion

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