A novel EXT2 frameshift mutation identified in a family with multiple osteochondromas
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DOI: 10.3892/ol.2018.9248
Abstract: Multiple osteochondromas (MO) is an autosomal inherited disease that is characterized by benign bone tumors. However, the underlying mechanism of MO at a molecular level requires further investigation. The majority of mutations associated with MO… read more here.
Keywords: multiple osteochondromas; family; frameshift mutation; mutation ... See more keywords