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

Learn More →

Corrigendum

Corrigendum A Novel Homozygous Nonsense Mutation in the PVRL4 Gene and Expansion of Clinical Spectrum of EDSS1In this article published in Volume 79 Issue 2 (March 2015), the figure and the mutation name used in the legend for Figure  were incorrect. The correct figure and its legend are now provided below:4Mutation 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]REFERENCERaza, 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. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Annals of Human Genetics Wiley

Corrigendum

Annals of Human Genetics , Volume 82 (1) – Jan 1, 2018

Loading next page...
 
/lp/wiley/corrigendum-ZviV5pbcBT

References (1)

Publisher
Wiley
Copyright
Copyright © 2018 John Wiley & Sons Ltd/University College London
ISSN
0003-4800
eISSN
1469-1809
DOI
10.1111/ahg.12237
Publisher site
See Article on Publisher Site

Abstract

A Novel Homozygous Nonsense Mutation in the PVRL4 Gene and Expansion of Clinical Spectrum of EDSS1In this article published in Volume 79 Issue 2 (March 2015), the figure and the mutation name used in the legend for Figure  were incorrect. The correct figure and its legend are now provided below:4Mutation 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]REFERENCERaza, 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.

Journal

Annals of Human GeneticsWiley

Published: Jan 1, 2018

There are no references for this article.