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Novel exostosin-2 mutation identified in a Chinese family with hereditary multiple osteochondroma
Hereditary multiple osteochondroma (HMO) is an autosomal dominant genetic disorder characterized by multiple outgrowing bony tumors capped by cartilage, generally affecting the metaphyses. The disease is known as hereditary multiple exostoses, familial exostosis, multiple cartilaginous exostoses or...
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| Publicado no: | Oncol Lett |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5835906/ https://ncbi.nlm.nih.gov/pubmed/29541207 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/ol.2018.7838 |
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