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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...

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Main Authors: O'HARA, A M, FERNIE, B A, MORAN, A P, WILLIAMS, Y E, CONNAUGHTON, J J, ORREN, A, HOBART, M J
格式: Artigo
語言:Inglês
出版: Blackwell Publishing Ltd 1998
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在線閱讀: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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