A novel mutation for TAP deficiency and its possible association with Toxoplasmosis. [electronic resource]
Producer: 20060926Description: 219-22 p. digitalISSN:- 1383-5769
- ATP Binding Cassette Transporter, Subfamily B, Member 2
- ATP-Binding Cassette Transporters -- genetics
- Adult
- B-Lymphocytes -- immunology
- Child
- Codon, Nonsense
- Consanguinity
- Female
- Genes, MHC Class I
- Humans
- Immunoglobulin A -- blood
- Immunoglobulin G -- blood
- Leukocytes, Mononuclear
- Male
- Point Mutation
- Toxoplasmosis -- genetics
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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