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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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Bibliografski detalji
Glavni autori: O'HARA, A M, FERNIE, B A, MORAN, A P, WILLIAMS, Y E, CONNAUGHTON, J J, ORREN, A, HOBART, M J
Format: Artigo
Jezik:Inglês
Izdano: Blackwell Publishing Ltd 1998
Teme:
Online pristup: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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