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FUT1 mutations responsible for the H-deficient phenotype in the Polish population, including the first example of an abolished start codon
by
Michalewska, Bogumila
,
Olsson, Martin L.
,
Naremska, Grazyna
,
Walenciak, Jolanta
,
Hult, Annika K.
,
Ozog, Agnieszka
,
Guz, Katarzyna
,
Brojer, Ewa
,
Storry, Jill R.
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Blood transfusion = Trasfusione del sangue
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Blood Transfusion = Trasfusione Del Sangue
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Abo Blood-Group System - Biosynthesis
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Abo Blood-Group System - Genetics
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Alleles
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Brief Communication
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Chromosomes, Human, Pair 19 - Genetics
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Chromosomes, Human, Pair 19 - Metabolism
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Clinical Laboratory Medicine
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Clinical Medicine
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Codon, Initiator
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Female
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Fucosyltransferases - Biosynthesis
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Fucosyltransferases - Genetics
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Galactoside 2-Alpha-L-Fucosyltransferase
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Gene Expression Regulation, Enzymologic
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Hematology
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Heterozygote
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Humans
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Klinisk Laboratoriemedicin
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Klinisk Medicin
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