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Complete functional C1q deficiency associated with systemic lupus erythematosus (SLE).

A complete functional deficiency of C1q is described in a patient suffering from SLE. From reduced plasma C1 activity of the parents a hereditary trait was assumed. The defective C1q molecule was haemolytically inactive, did not bind to immune complexes, and was not recognized by the monocyte C1q re...

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Detaylı Bibliyografya
Asıl Yazarlar: Kirschfink, M, Petry, F, Khirwadkar, K, Wigand, R, Kaltwasser, J P, Loos, M
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1993
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1534221/
https://ncbi.nlm.nih.gov/pubmed/7900940
Etiketler: Etiketle
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