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A novel mutation in the VHL gene in a Chinese family with von Hippel-Lindau disease
BACKGROUND: Von Hippel-Lindau (VHL) disease is an autosomal dominant inherited cancer syndrome, and VHL is identified as a tumor suppressor gene. The main objective of this study was to identify disease-causing mutations in a Chinese family affected with VHL disease. METHODS: Genomic DNA was extract...
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| izdano v: | BMC Med Genet |
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| Main Authors: | , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BioMed Central
2018
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6258150/ https://ncbi.nlm.nih.gov/pubmed/30477447 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-018-0716-4 |
| Oznake: |
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