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gamma Heavy chain disease in man: cDNA sequence supports partial gene deletion model.
Human gamma heavy chain disease (HCD) is characterized by the presence in serum of a short monoclonal Ig gamma chain unattached to light chains. Although most HCD proteins have internal deletions, in some the defect is NH2-terminal. The OMM gamma 3 HCD serum protein is of the latter type, having und...
Tallennettuna:
| Julkaisussa: | Proc Natl Acad Sci U S A |
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| Päätekijät: | , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
National Academy of Sciences
1982
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC346395/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6808505/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.79.10.3260 |
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