Importance of the third thrombospondin repeat of C6 for terminal complement complex assembly.

Por Würzner, R, Mewar, D, Fernie, B A, Hobart, M J, Lachmann, P J
Publicado em 1995

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

Por Fernie, B A, Hobart, M J, Delbridge, G, Potter, P C, Orren, A, Lachmann, P J
Publicado em 1994

Properties of a low molecular weight complement component C6 found in human subjects with subtotal C6 deficiency.

Por Orren, A, Würzner, R, Potter, P C, Fernie, B A, Coetzee, S, Morgan, B P, Lachmann, P J
Publicado em 1992

Molecular basis of subtotal complement C6 deficiency. A carboxy-terminally truncated but functionally active C6.

Por Würzner, R, Hobart, M J, Fernie, B A, Mewar, D, Potter, P C, Orren, A, Lachmann, P J
Publicado em 1995

Difficulties in the ascertainment of C9 deficiency: lessons to be drawn from a compound heterozygote C9-deficient subject

Por HOBART, M J, FERNIE, B A, WÜRZNER, R, OLDROYD, R G, HARRISON, R A, JOYSEY, V, LACHMANN, P J
Publicado em 1997

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

Por O'HARA, A M, FERNIE, B A, MORAN, A P, WILLIAMS, Y E, CONNAUGHTON, J J, ORREN, A, HOBART, M J
Publicado em 1998

How partial C7 deficiency with chronic and recurrent bacterial infections can mimic total C7 deficiency: temporary restoration of host C7 levels following plasma transfusion.

Por Würzner, R, Platonov, A E, Beloborodov, V B, Pereverzev, A I, Vershinina, I V, Fernie, B A, Hobart, M J, Lachmann, P J, Orren, A
Publicado em 1996