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...
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| 出版年: | Proc Natl Acad Sci U S A |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
National Academy of Sciences
1982
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| 主題: | |
| オンライン･アクセス: | 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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