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A novel EXT2 frameshift mutation identified in a family with multiple osteochondromas

Multiple osteochondromas (MO) is an autosomal inherited disease that is characterized by benign bone tumors. However, the underlying mechanism of MO at a molecular level requires further investigation. The majority of mutations associated with MO occur in the exostosin glycosyltransferase genes (EXT...

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書目詳細資料
發表在:Oncol Lett
Main Authors: Chen, Zhonghua, Bi, Qing, Kong, Mingxiang, Cao, Li, Ruan, Weiwei
格式: Artigo
語言:Inglês
出版: D.A. Spandidos 2018
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC6144921/
https://ncbi.nlm.nih.gov/pubmed/30250583
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/ol.2018.9248
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