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Corrigendum for Williamson et al., Hum. Mol. Genet. 15 (9) 1413-1422.
Human Molecular Genetics 2006 15(12):2030; doi:10.1093/hmg/ddl127
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© The Author 2006. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

CORRIGENDUM

Mutations in SOX2 cause anophthalmia–esophageal–genital (AEG) syndrome

Kathleen A. Williamson, Ann M. Hever, Joe Rainger, R. Curtis Rogers, Alex Magee, Zdenek Fiedler, Wee Teik Keng, Freddie H. Sharkey, Niolette McGill, Clare J. Hill, Adele Schneider, Mario Messina, Peter D. Turnpenny, Judy A. Fantes, Veronica van Heyningen and David R. FitzPatrick

Human Molecular Genetics (2006) 15, 1413–1422; doi:10.1093/hmg/ddl064

Table 1 has been reproduced as a corrigendum due to errors in the original publication.


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  		Table 1. Phenotypes and SOX2 mutations in AEG syndrome
 


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This Article
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