Corrigendum: Novel single base polymorphisms and rare sequence variants in the laminin ?2-chain coding region detected by RNA/SSCP analysis

CORRIGENDUM: The Human Mutation Mutation and Polymorphism Report (MPR) titled "Novel single base polymorphisms and rare sequence variants in the laminin ±2-chain coding region detected by RNA/SSCP analysis" by Panicker et al., which is published online (MPR #38, 1998), was presented in incomplete form. This was due to a miscommunication between the Editorial Office and the authors. Please consider the new version indicated here (MPR #43, 1999) as the complete published manuscript. This version, in addition to completing some information originally requested in review, also corrects a typographical error regarding the electrophoresis conditions; viz., the gel runs were performed at 4°C (page 2, MPR #38, 1998).; Authors and readers should note that, because of our need to maintain the same archival integrity of our on-line journal articles afforded our print journal articles, no on-line manuscripts can be pulled off-line, corrected, and subsequently uploaded. However, we are able to publish on-line errata and corrigenda, at the discretion of the Editors.; To facilitate the prompt dissemination of accurate scientific data, we will electronically link the original on-line articles and related corrigenda/errata as appropriate. We cannot be held responsible, however, for instigating similar links between errata or corrigenda within Medline/PubMed or other literary indexing services.; Mark H. Paalman, Ph.D.; Managing Editor, Human Mutation; John Wiley & Sons, Inc., New York