Hereditary deficiency of the seventh component of complement.

Deficiency of the seventh component of complement has been found in the serum of a 42-yr-old Caucasian woman who has Raynaud's phenomenon, sclerodactyly, and telangiectasia. Partial deficiency was found in the serum of the patient's parents and children, indicating a pattern of inheritance of autoso...

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Dades bibliogràfiques

Publicat a:	J Clin Invest
Autors principals:	Boyer, J T, Gall, E P, Norman, M E, Nilsson, U R, Zimmerman, T S
Format:	Artigo
Idioma:	Inglês
Publicat:	American Society for Clinical Investigation 1975
Matèries:	Research Article
Accés en línia:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC301946/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1099121/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI108170
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