Source:http://linkedlifedata.com/resource/umls/id/C0085113
MSH: Tumor suppressor genes located on the long arm of human chromosome 17 in the region 17q11.2. Mutation of these genes is thought to cause NEUROFIBROMATOSIS 1, Watson syndrome, and LEOPARD syndrome.,NCI: This gene plays a role in signal transduction and cytoskeletal remodeling.