Predisposition to atypical hemolytic uremic syndrome involves the concurrence of different susceptibility alleles in the regulators of complement activation gene cluster in 1q32

Human Molecular Genetics14, 703–712 (2005)

Some MCP SNP and aHUS-associated MCP mutation names listed throughout the paper were accidently referred to the first nucleotide of a human MCPcDNA sequence with an anomalous transcription start site (GenBank ID#NM002389). The authors would like to apologize for this error. The authors' reference MCP_cDNA sequence is that reported by Cui et al. J. Immunol., 151, 4137–4146 (1993).

• Name in the paper Correct name

• c.573A>G c.522A>G

• c.903-907del c.852-856del

• c.2232T>C c.2181T>C

• c.463C>T (R103T) c.412C>T (R103W)