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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Detalhes bibliográficos
Publicado no:Proc Natl Acad Sci U S A
Main Authors: Alexander, A, Steinmetz, M, Barritault, D, Frangione, B, Franklin, E C, Hood, L, Buxbaum, J N
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 1982
Assuntos:
Research Article
Acesso em linha: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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