Related Articles

• A novel splice mutation induces exon skipping of the EXT1 gene in patients with hereditary multiple exostoses
• Identification of a novel mutation in the EXT1 gene from a patient with multiple osteochondromas by exome sequencing
• Whole‑exome sequencing identifies a novel mutation of SLC20A2 (c.C1849T) as a possible cause of hereditary multiple exostoses in a Chinese family
• Novel EXT1 mutation identified in a pedigree with hereditary multiple exostoses
• Clinical survey of a pedigree with hereditary multiple exostoses and identification of EXT‑2 gene deletion mutation