Correction

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With regard to the December 2006 article entitled “First case of homozygous C1 inhibitor deficiency” (2006;118:1330-5), the authors regret that there was an error in the nomenclature of the mutation reported in the original article. The nomenclature c.1576T>G is not correct. It should be c.1385T>G according to the recommendations of the Human Genome Variation Society. The numbering 1576 refers to the nucleotide position in the reference sequence NM_000062.2 GI:73858567, whereas the numbering 1385 considers nucleotide number 1 as the A of the ATG-translation initiation codon.