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HUMAN MUTATION Mutation in Brief #576 (2002) O nline MUTATION IN BRIEF ERRATUM Detection of C1 Inhibitor (SERPING1/C1NH) Mutations in Exon 8 In Patients With Hereditary Angioedema: Evidence For 10 Novel Mutations † † Alvaro Blanch , Olga Roche , Eduardo López-Granados, Gumersindo Fontán, and Margarita López-Trascasa* Unidad de Inmunología, Hospital Universitario "La Paz", Paseo de la Castellana, 261, 28046 Madrid, Spain The first two authors contributed equally to this work *Correspondence to: Margarita López-Trascasa, Unidad de Inmunología, Hospital Universitario "La PAZ", Paseo de la Castellana, 261, 28046 Madrid, Spain; Tel.: 34917277238; Fax: 349172727095; E-mail: mlopeztrascasa@hulp.insalud.es Grant sponsor: Fondo de Investigaciones Sanitarias (FIS); Grant number: 00/0216; Instituto de Salud Carlos III and Comunidad Autónoma de Madrid (CAM); Grant number: 08.6/0028/2000; Grant sponsor: FIS (to O.R.); Grant Number: BEFI 00/9158. Communicated by Mark H. Paalman Original Reference: Blanch et al., Human Mutation, 20:405-406 (2002). The authors regret that there was an error in Table 2 on Page 4 of the original article. In patient DS, the nucleotide change 16838C>T is not correct. It should be 16838G>A, since this was the mutation at the antisense change. Received 23 April 2002; accepted revised manuscript 29 August 2002. © 2002 WILEY-LISS, INC. DOI: 10.1002/humu.9105
Human Mutation – Wiley
Published: Jan 1, 2003
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