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Molecular heterogeneity in deficiency of complement protein C2 type I.

Deficiency of the complement protein C2 (C2D), one of the most common genetic deficiencies of the complement system, is associated with rheumatological disorders and increased susceptibility to infection. Two types of C2D have been recognized, each in the context of specific major histocompatibility...

詳細記述

保存先:
書誌詳細
主要な著者: Wang, X, Circolo, A, Lokki, M L, Shackelford, P G, Wetsel, R A, Colten, H R
フォーマット: Artigo
言語:Inglês
出版事項: 1998
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC1364177/
https://ncbi.nlm.nih.gov/pubmed/9616367
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