Molecular analysis of the rare in(Lu) blood type: toward decoding the phenotypic outcome of haploinsufficiency for the transcription factor KLF1. [electronic resource]
Producer: 20130701Description: 221-8 p. digitalISSN:- 1098-1004
- Animals
- Blood Group Antigens -- genetics
- COS Cells
- Carrier Proteins -- genetics
- Cell Adhesion Molecules -- blood
- Chlorocebus aethiops
- Erythrocytes -- metabolism
- Female
- Fetal Hemoglobin -- genetics
- Flow Cytometry
- Globosides -- genetics
- Haploinsufficiency
- Hemoglobin A2 -- genetics
- Humans
- Hyaluronan Receptors -- blood
- Kruppel-Like Transcription Factors -- genetics
- Lutheran Blood-Group System -- blood
- Male
- Mutation, Missense
- Nuclear Proteins -- genetics
- Pedigree
- Phenotype
- Polymorphism, Single Nucleotide
- Proto-Oncogene Proteins c-myb -- genetics
- Repressor Proteins
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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