Get 20M+ Full-Text Papers For Less Than $1.50/day. Start a 14-Day Trial for You or Your Team.

Learn More →

Erratum: Detection of C1 inhibitor (SERPING1/C1NH) mutations in exon 8 in patients with hereditary angioedema: evidence for 10 novel mutations

Erratum: Detection of C1 inhibitor (SERPING1/C1NH) mutations in exon 8 in patients with... 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 http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Human Mutation Wiley

Erratum: Detection of C1 inhibitor (SERPING1/C1NH) mutations in exon 8 in patients with hereditary angioedema: evidence for 10 novel mutations

Download PDF
1 page

Loading next page...
 
/lp/wiley/erratum-detection-of-c1-inhibitor-serping1-c1nh-mutations-in-exon-8-in-0n3d3mL62W

References (0)

References for this paper are not available at this time. We will be adding them shortly, thank you for your patience.

Publisher
Wiley
Copyright
Copyright © 2003 Wiley Subscription Services, Inc., A Wiley Company
ISSN
1059-7794
eISSN
1098-1004
DOI
10.1002/humu.9105
Publisher site
See Article on Publisher Site

Abstract

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

Journal

Human Mutation – Wiley

Published: Jan 1, 2003

There are no references for this article.