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S. I. Raza, R. N. Dar, A. A. Shah, W. Ahmad (2013)
A novel homozygous nonsense mutation in the PVRL4 gene and expansion of clinical spectrum of EDSS1, 79
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.
Annals of Human Genetics – Wiley
Published: Jan 1, 2018
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