A congenital disorder of deglycosylation: Biochemical characterization of N-glycanase 1 deficiency in patient fibroblasts.

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Published in Glycobiology on April 21, 2015

Authors

Ping He1, Jeff E Grotzke2, Bobby G Ng1, Murat Gunel3, Hamed Jafar-Nejad4, Peter Cresswell2, Gregory M Enns5, Hudson H Freeze6

Author Affiliations

1: Human Genetics Program, Sanford Children's Health Research Center, Sanford Burnham Medical Research Institute, 10901 North Torrey Pines Road, La Jolla, CA 92037, USA.
2: Department of Immunobiology, Yale University, School of Medicine, New Haven, CT 06520-8011, USA.
3: Yale Program on Neurogenetics, Departments of Neurosurgery, Neurobiology and Genetics, Yale University, School of Medicine, New Haven, CT 06510, USA.
4: Department of Molecular and Human Genetics, Program in Developmental Biology, Baylor College of Medicine, Houston, TX 77030, USA.
5: Department of Pediatrics, Division of Medical Genetics, Lucile Packard Children's Hospital, Stanford University, Stanford, CA 94304, USA.
6: Human Genetics Program, Sanford Children's Health Research Center, Sanford Burnham Medical Research Institute, 10901 North Torrey Pines Road, La Jolla, CA 92037, USA hudson@sanfordburnham.org.

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