Corrigendum.

Abstract

Annals of Human GeneticsVolume 82, Issue 1 p. 52-52 CORRIGENDUMFree Access Corrigendum This article corrects the following: A Novel Homozygous Nonsense Mutation in the PVRL4 Gene and Expansion of Clinical Spectrum of EDSS1 Syed Irfan Raza, Rashid Nasser Dar, Anwar Ali Shah, Wasim Ahmad, Volume 79Issue 2Annals of Human Genetics pages: 92-98 First Published online: December 22, 2014 First published: 19 December 2017 https://doi.org/10.1111/ahg.12237AboutSectionsPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat A Novel Homozygous Nonsense Mutation in the PVRL4 Gene and Expansion of Clinical Spectrum of EDSS1 In this article published in Volume 79 Issue 2 (March 2015), the figure and the mutation name used in the legend for Figure 4 were incorrect. The correct figure and its legend are now provided below: Figure 4Open in figure viewerPowerPoint Mutation analysis of the PVRL4 gene. DNA sequence analysis of the PVRL4 gene shows a substitution of C with T at nucleotide position 181 (c.181C > T; p.Gln61*). (A) Homozygous mutant nucleotide sequence in an affected family member. (B) Heterozygous nucleotide sequence in a carrier. (C) Homozygous wild-type nucleotide sequence in an unaffected family member [Color figure can be viewed at wileyonlinelibrary.com] REFERENCE Raza, S. I., Dar, R. N., Shah, A. A., & Ahmad, W. (2013). A novel homozygous nonsense mutation in the PVRL4 gene and expansion of clinical spectrum of EDSS1. Annals of Human Genetics, 79, 92– 98. Volume82, Issue1January 2018Pages 52-52 FiguresReferencesRelatedInformation