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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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Dades bibliogràfiques
Publicat a:Oncol Lett
Autors principals: Ruan, Weiwei, Cao, Li, Chen, Zhonghua, Kong, Mingxiang, Bi, Qing
Format: Artigo
Idioma:Inglês
Publicat: D.A. Spandidos 2018
Matèries:
Accés en línia: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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