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Identification of a novel frameshift mutation of the EXT2 gene in a family with multiple osteochondroma
Multiple osteochondroma (MO), also known as multiple hereditary exostoses, is an autosomal dominant skeletal disorder with characteristic multiple cartilage-capped tumours (osteochondromas or exostoses) growing outward from the metaphyseal region of the long tubular bones. Mutations in exostosin gly...
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| Publicat a: | Oncol Lett |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
D.A. Spandidos
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4727190/ https://ncbi.nlm.nih.gov/pubmed/26870176 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/ol.2015.3844 |
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