Homozygous human TAP peptide transporter mutation in HLA class I deficiency. [electronic resource]
Producer: 19940802Description: 237-41 p. digitalISSN:- 0036-8075
- ATP Binding Cassette Transporter, Subfamily B, Member 2
- ATP Binding Cassette Transporter, Subfamily B, Member 3
- ATP-Binding Cassette Transporters
- Adolescent
- Amino Acid Sequence
- Antigens, CD -- analysis
- Antigens, CD1
- Base Sequence
- Carrier Proteins -- analysis
- Child
- Female
- Histocompatibility Antigens Class I -- analysis
- Homozygote
- Humans
- Immunologic Deficiency Syndromes -- genetics
- Killer Cells, Natural -- immunology
- Langerhans Cells -- immunology
- Leukocyte Count
- Lymphocytes -- immunology
- Male
- Molecular Sequence Data
- Mutation
- T-Lymphocyte Subsets -- immunology
- T-Lymphocytes, Cytotoxic -- immunology
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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