Works matching IS 10597794 AND DT 2006 AND VI 27 AND IP 12
Results: 9
Chronic granulomatous disease caused by mutations other than the common GT deletion in NCF1, the gene encoding the p47<sup>phox</sup> component of the phagocyte NADPH oxidase.
- Published in:
- Human Mutation, 2006, v. 27, n. 12, p. 1218, doi. 10.1002/humu.20413
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- Article
Activation-induced cytidine deaminase: structure-function relationship as based on the study of mutants.
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- Human Mutation, 2006, v. 27, n. 12, p. 1185, doi. 10.1002/humu.20414
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- Article
Bioinformatic analysis of protein structure-function relationships: case study of leukocyte elastase ( ELA2) missense mutations.
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- Human Mutation, 2006, v. 27, n. 12, p. 1230, doi. 10.1002/humu.20407
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- Article
The IMGT/HLA and IPD databases.
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- Human Mutation, 2006, v. 27, n. 12, p. 1192, doi. 10.1002/humu.20406
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- Article
Molecular approaches in the diagnosis of primary immunodeficiency diseases.
- Published in:
- Human Mutation, 2006, v. 27, n. 12, p. 1163, doi. 10.1002/humu.20412
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- Article
Immunodeficiency mutation databases (IDbases).
- Published in:
- Human Mutation, 2006, v. 27, n. 12, p. 1200, doi. 10.1002/humu.20405
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- Article
Focus on immunogenetics: diagnosis, molecular genetics, mutations, and diseases.
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- Human Mutation, 2006, v. 27, n. 12, p. 1161, doi. 10.1002/humu.20427
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- Article
RAG-dependent primary immunodeficiencies.
- Published in:
- Human Mutation, 2006, v. 27, n. 12, p. 1174, doi. 10.1002/humu.20408
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- Article
BTKbase: the mutation database for X-linked agammaglobulinemia.
- Published in:
- Human Mutation, 2006, v. 27, n. 12, p. 1209, doi. 10.1002/humu.20410
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- Article