Cohen Syndrome-associated Protein, COH1, Is a Novel, Giant Golgi Matrix Protein Required for Golgi Integrity

High frequency of COH1 intragenic deletions and duplications detected by MLPA in patients with Cohen syndrome

(2010) Veronica Parri et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Search for the best indicators for the presence of a VPS13B gene mutation and confirmation of diagnostic criteria in a series of 34 patients genotyped for suspected Cohen syndrome

(2010) S. El Chehadeh et al.   JOURNAL OF MEDICAL GENETICS

Rab6 and myosin II at the cutting edge of membrane fission

(2010) Carmen Valente et al.   NATURE CELL BIOLOGY

TGN golgins, Rabs and cytoskeleton: regulating the Golgi trafficking highways

(2010) Bruno Goud et al.   TRENDS IN CELL BIOLOGY

Expanded mutational spectrum in Cohen syndrome, tissue expression, and transcript variants ofCOH1

(2008) Wenke Seifert et al.   HUMAN MUTATION

GRASP55 Regulates Golgi Ribbon Formation

(2008) Timothy N. Feinstein et al.   MOLECULAR BIOLOGY OF THE CELL