Related Articles
Hereditary multiple and isolated sporadic exostoses in the same kindred: Identification of the causative gene (EXT2) and detection of a new mutation, nt112delAT, that distinguishes the two phenotypes
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
Identification of a novel ANK1 mutation in a Chinese family with hereditary spherocytosis: A case report
A novel splice mutation induces exon skipping of the EXT1 gene in patients with hereditary multiple exostoses