A new genetic background for the Jr(a-) blood group phenotype caused by the ABCG2*439T allele encoding a p.Arg147Trp change. [electronic resource]
Producer: 20180322Description: 3063-3064 p. digitalISSN:- 1537-2995
- ATP Binding Cassette Transporter, Subfamily G, Member 2 -- genetics
- Alleles
- Amino Acid Substitution
- Blood Group Antigens -- genetics
- Coombs Test
- Diseases in Twins -- genetics
- Exons -- genetics
- Female
- Genotype
- Humans
- Male
- Mutation, Missense
- Neoplasm Proteins -- genetics
- Pedigree
- Phenotype
- Point Mutation
- Sequence Analysis, DNA
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Publication Type: Journal Article
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