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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Autors principals: Alexander, A, Steinmetz, M, Barritault, D, Frangione, B, Franklin, E C, Hood, L, Buxbaum, J N
Format: Artigo
Idioma:Inglês
Publicat: 1982
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC346395/
https://ncbi.nlm.nih.gov/pubmed/6808505
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