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C6 haplotypes: associations of a Dde I site polymorphism to complement deficiency genes and the Msp I restriction fragment length polymorphism (RFLP)

Complement C6 has a common charge polymorphism designated A and B with gene frequencies of 0.65 and 0.35. The probable molecular basis for this is a Glu (C6A) for Ala (C6B) substitution at amino acid position 98, and is detected by digestion with the restriction enzyme Dde I of a polymerase chain re...

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Bibliografske podrobnosti
Main Authors: Fernie, B A, Hobart, M J, Delbridge, G, Potter, P C, Orren, A, Lachmann, P J
Format: Artigo
Jezik:Inglês
Izdano: 1994
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC1534913/
https://ncbi.nlm.nih.gov/pubmed/7508350
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