Publication | Open Access

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

Cohen Syndrome IsMolecular PhysiologyDisease MechanismMendelian DisorderGenetic DisorderGeneticsMolecular BiologyMolecular GeneticsDisease Gene IdentificationProtein TransportTransmembrane ProteinMedicineIntracellular Protein Transport