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WRN Cys1367Arg polymorphism is not associated with skull base chordoma
Skull base chordoma is a rare tumor with unknown risk factors. Werner syndrome, which is caused by a mutation in the WRN gene, is a disease of progeria, resembling the pathological process of aging. The present study aimed to provide data on the possible association between skull base chordoma and t...
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| Main Authors: | , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4051466/ https://ncbi.nlm.nih.gov/pubmed/24944800 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/br.2014.275 |
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