Mutation spectrum of EXT1 and EXT2 in the Saudi patients with hereditary multiple exostoses

Hereditary Multiple Exostoses (HME), also known as Multiple Osteochondromas (MO) is a rare genetic disorder characterized by multiple benign cartilaginous bone tumors, which are caused by mutations in the gene...

Source: Orphanet Journal of Rare Diseases - February 25, 2021 Category: Internal Medicine Authors: Zayed Al-Zayed, Roua A. Al-Rijjal, Lamya Al-Ghofaili, Huda A. BinEssa, Rajeev Pant, Anwar Alrabiah, Thamer Al-Hussainan, Minjing Zou, Brian F. Meyer and Yufei Shi Tags: Research Source Type: research