Skip to main content
. 2006 Apr 18;108(4):1267–1279. doi: 10.1182/blood-2005-10-007252

Table 4.

IF gene mutations in non-Stx–HUS patients from our registry

Exon/intron, subject/family code Mutation Effect Subgroups Inheritance IF serum levels, %*
Ex V
    S211 117 719C > G A240G Sporadic Heterozygote 98
Ex IX
    F215 010 949C > T R317W Familial Heterozygote ND
    F216 010 949C > T R317W Familial Heterozygote 98
Ex XII
    S199 192 (1446-1450)delTTCAC L484V + Q485G + W486Stop Sporadic Heterozygote 77
Int 12
    S214 150 1534 + 5G > T Splice score decrease from 93 to 86 Sporadic Heterozygote 103
Ex XIII
    F118 034 1555G > A D519N Familial Heterozygote ND
    F119 034 1555G > A D519N Familial Heterozygote ND

ND indicates not done.

*

IF serum levels were measured by ELISA assay as described by Fremeaux-Bacchi et al18 (normal range, 70%-130%).

Patient carrying both MCP and IF mutations.