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Corrigendum for Esparza-Gordillo et al., Hum. Mol. Genet. 14 (5) 703-712.
Human Molecular Genetics 2005 14(8):1107; doi:10.1093/hmg/ddi099
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© The Author 2005. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oupjournals.org

CORRIGENDUM

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

Jorge Esparza-Gordillo, Elena Goicoechea de Jorge, Alfonso Buil, Luis Carreras Berges, Margarita López-Trascasa, Pilar Sánchez-Corral and Santiago Rodríguez de Córdoba

Human Molecular Genetics 14, 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)


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