Mutations in Kruppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expression. [electronic resource]
Producer: 20140509Description: 1586-95 p. digitalISSN:- 1528-0020
- Adolescent
- Adult
- Amino Acid Sequence
- Anemia, Hemolytic -- blood
- Child
- Child, Preschool
- Conserved Sequence
- Erythrocyte Indices
- Erythrocytes -- metabolism
- Female
- Fetal Hemoglobin -- chemistry
- Gene Expression Regulation
- Gene Order
- Humans
- Infant
- Kruppel-Like Transcription Factors -- genetics
- Male
- Molecular Sequence Data
- Mutation
- Protein Binding
- Protein Interaction Domains and Motifs
- Sequence Alignment
- Transfusion Reaction
- Young Adult
- alpha-Globins -- metabolism
- beta-Globins -- metabolism
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.