Christian Körner

发表

Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as a GDP-fucose transporter deficiency

Amos Etzioni, E. Hartmann, K. Figura, 2001, Nature Genetics.

The mitochondrial contact site complex, a determinant of mitochondrial architecture

Matthias Mann, Walter Neupert, Johannes Kaesmacher, 2011, The EMBO journal.

Gene identification in the congenital disorders of glycosylation type I by whole-exome sequencing.

Christian Gilissen, Alexander Hoischen, Ron A Wevers, 2012, Human molecular genetics.

Glycomic Characterization of Induced Pluripotent Stem Cells Derived from a Patient Suffering from Phosphomannomutase 2 Congenital Disorder of Glycosylation (PMM2-CDG)

Erdmann Rapp, Udo Reichl, Samanta Cajic, 2016, Molecular & Cellular Proteomics.