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C7 deficiency in an Irish family: a deletion defect which is predominant in the Irish

Human deficiencies of terminal complement components are known to be associated with increased susceptibility to Neisseria meningitidis infection. Polymorphic DNA marker studies in complement deficient investigations allow identification of haplotypes associated with the deficiency and enable the po...

詳細記述

保存先:
書誌詳細
主要な著者: O'HARA, A M, FERNIE, B A, MORAN, A P, WILLIAMS, Y E, CONNAUGHTON, J J, ORREN, A, HOBART, M J
フォーマット: Artigo
言語:Inglês
出版事項: Blackwell Publishing Ltd 1998
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC1905122/
https://ncbi.nlm.nih.gov/pubmed/9844043
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1046/j.1365-2249.1998.00737.x
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