Identification of a Novel FUT1 Allele with c.425G > A on the FUT1*01 Allele Background
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s12288-024-01838-3.pdf
Reference12 articles.
1. Oriol R, Candelier JJ, Mollicone R (2000) Molecular genetics of H. Vox Sang 78:105–108
2. International Society of Blood Transfusion (2024) https://www.isbtweb.org/resource/tableofbloodgroupantigenswithinsystems.html. Accessed 11 June 2024
3. Wagner FF, Flegel WA (1997) Polymorphism of the h allele and the population frequency of sporadic nonfunctional alleles. Transfusion 37:284–290
4. Blumenfeld OO, Patnaik SK (2004) Allelic genes of blood group antigens: a source of human mutations and cSNPs documented in the Blood Group Antigen Gene Mutation Database. Hum Mutat 23:8–16
5. Shao LN, Yang YC, Xia YX, Li CX, Zhou SH, Liang XH (2024) Novel missense mutation c.797T > C (p.Met266Thr) gives rise to the rare B(A) phenotype in a Chinese family. Vox Sang. https://doi.org/10.1111/vox.13591
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