FUT1 Mutations Responsible for the H-deficient Phenotype in the Polish Population, Including the First Example of an Abolished Start Codon

Overview

Journal Blood Transfus

Specialty Hematology

Date 2016 Nov 29

PMID 27893357

Citations 2

Authors

Bogumila Michalewska

Martin L Olsson

Grazyna Naremska

Jolanta Walenciak

Annika K Hult

Agnieszka Ozog

Katarzyna Guz

Ewa Brojer

Jill R Storry

Affiliations

Soon will be listed here.

Citing Articles

Genotyping of the rare Para-Bombay blood group in southern Thailand.

Rattanapan Y, Charong N, Narkpetch S, Chareonsirisuthigul T Hematol Transfus Cell Ther. 2022; 45(4):449-455.

PMID: 36241527 PMC: 10627842. DOI: 10.1016/j.htct.2022.08.004.

FUT1 mutations responsible for the H-deficient phenotype in the Polish population, including the first example of an abolished start codon.

Michalewska B, Olsson M, Naremska G, Walenciak J, Hult A, Ozog A Blood Transfus. 2016; 16(1):101-104.

PMID: 27893357 PMC: 5770320. DOI: 10.2450/2016.0135-16.

References

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Michalewska B, Olsson M, Naremska G, Walenciak J, Hult A, Ozog A . FUT1 mutations responsible for the H-deficient phenotype in the Polish population, including the first example of an abolished start codon. Blood Transfus. 2016; 16(1):101-104. PMC: 5770320. DOI: 10.2450/2016.0135-16. View

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