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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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| 發表在: | Oncol Lett |
|---|---|
| Main Authors: | , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
D.A. Spandidos
2018
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| 主題: | |
| 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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