A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If)Christian Kranz, Thorsten Marquardt, Jonas Denecke et al.|Journal of Clinical Investigation|2001Cited by 130
COG8 deficiency causes new congenital disorder of glycosylation type IIhChristian Kranz, Hudson H. Freeze, Yoshiaki Miura et al.|Human Molecular Genetics|2007Cited by 122
Endoglycosidase and Glycoamidase Release of N‐Linked GlycansHudson H. Freeze, Christian Kranz|Current Protocols in Protein Science|2010Cited by 103
Expanding spectrum of congenital disorder of glycosylation Ig (CDG‐Ig): Sibs with a unique skeletal dysplasia, hypogammaglobulinemia, cardiomyopathy, genital malformations, and early lethalityChristian Kranz, Hudson H. Freeze, Alice Basinger et al.|American Journal of Medical Genetics Part A|2007Cited by 93
Endoglycosidase and Glycoamidase Release of N‐Linked GlycansHudson H. Freeze, Christian Kranz|Current Protocols in Molecular Biology|2010Cited by 64