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Article

C7 M/N protein polymorphism typing applied to inherited deficiencies of human complement proteins C6 and C7.

Clinical and experimental immunology - 1 Sept 1992

Würzner R, Rance N, Potter P C, Hendricks M L, Lachmann P J, Orren A

Abstract excerpt

C7 M/N typing, the determination of the complement component C7 M/N phenotypes, was successfully used in family studies to trace haplotypes bearing C7 deficiency genes. Furthermore, it was shown to be preferable to C7 allotyping based on isoelectric focusing (IEF) since it distinguishes two common alleles (C7*M and C7*N), whereas one common C7 IEF allele (C7*1) predominates in most populations. It is also the...

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Identifiers

PMID: 1516263
DOI: 10.1111/j.1365-2249.1992.tb06985.x
PMCID: PMC1554460

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