Cohen syndrome is caused by mutations in a novel gene, COH1, encoding a transmembrane protein with a presumed role in vesicle-mediated sorting and intracellular protein transport - Kolehmainen, J; Black, GCM; Saarinen, A; Chandler, K; Clayton-Smith, J; Traskelin, A; Perveen, R (Am J Hum Genet, 2003)
et al.