Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum–associated degradation pathway
Gregory M. Enns(Lucile Packard Children's Hospital), David B. Goldstein(Electronic BioSciences (United States)), Anna C. Need(University of Pavia), Hudson H. Freeze(Discovery Institute), Mena Scavina(Alfred I. duPont Hospital for Children), Rhonda S. Walter(Alfred I. duPont Hospital for Children), Huda Y. Zoghbi(Howard Hughes Medical Institute), Brett H. Graham(Baylor College of Medicine), Tina M. Cowan(Stanford University), M Snyder(Stanford University), Audrey Bibb(Emory University), Christian P. Schaaf(University of Cologne), Angélica Oviedo(Pediatric Hospital "Baca Ortiz"), Farah Zahir(University of British Columbia), Rebecca Crimian(Duke Medical Center), Atul J. Butte(University of California, San Francisco), Madhuri Hegde(Emory University), Matthew N. Bainbridge(Baylor College of Medicine), Kelly Schoch(Duke University), Seán Boyle(Stanford University), Thomas Bast(Diakonie Kork), Michael J. Gambello(Emory University), Julia Platt(Lucile Packard Children's Hospital), Jonathan A. Bernstein(Bernstein Clinical Research Center), Rong Chen(Hebei North University), Ping He(Rutgers, The State University of New Jersey), Vandana Shashi(Duke Medical Center), Michael J. Clark(Stanford University), Richard A. Gibbs(Baylor College of Medicine), Rachel Cox(Lucile Packard Children's Hospital), Rajini Haraksingh(Stanford University), Melanie A. Jones(Emory University), Sylvie Langlois(University of British Columbia)
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