Gregory M. Enns MB, ChB, Vandana Shashi MD, MBBS, Matthew Bainbridge PhD, Michael J. Gambello MD, PhD, Farah R. Zahir PhD, Thomas Bast MD, Rebecca Crimian MS, Kelly Schoch MS, Julia Platt MS, Rachel Cox MS, Jonathan A. Bernstein MD, PhD, Mena Scavina DO, Rhonda S. Walter MD, Audrey Bibb MS, Melanie Jones PhD, Madhuri Hegde PhD, Brett H. Graham MD, PhD, Anna C. Need PhD, Angelica Oviedo MD, Christian P. Schaaf MD, PhD, Sean Boyle PhD, Atul J. Butte MD, PhD, Rui Chen, PhD, Rong Chen PhD, Michael J. Clark PhD, Rajini Haraksingh PhD, Tina M. Cowan PhD, FORGE Canada Consortium, Ping He MD, PhD, Sylvie Langlois MD, Huda Y. Zoghbi MD, Michael Snyder PhD, Richard A. Gibbs PhD, Hudson H. Freeze PhD, and David B. Goldstein PhD
Genet Med advance online publication, March 20, 2014; doi:10.1038/gim.2014.22
One of the authors of this article, Rui Chen, PhD, of Snyder Laboratory, Department of Genetics, Stanford University School of Medicine, Stanford, California, was mistakenly omitted from the author list. The authors regret the error.
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The online version of the original article can be found at 10.1038/gim.2014.22
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Correction: Corrigendum: Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum–associated degradation pathway. Genet Med 16, 568 (2014). https://doi.org/10.1038/gim.2014.61
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DOI: https://doi.org/10.1038/gim.2014.61