1.
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
by Kolehmainen, Juha
American journal of human genetics, 2003, Vol.72 (6), p.1359-1369
2.
Delineation of Cohen Syndrome Following a Large-Scale Genotype-Phenotype Screen
by Kolehmainen, Juha
American journal of human genetics, 2004, Vol.75 (1), p.122-127
3.
The genetics of cornea plana congenita
by Tahvanainen, E
Journal of medical genetics, 1996-02, Vol.33 (2), p.116-119
