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von Hippel–Lindau disease: A clinical and scientific review
The autosomal dominantly inherited disorder von Hippel–Lindau disease (VHL) is caused by germline mutations in the VHL tumour suppressor gene (TSG). VHL mutations predispose to the development of a variety of tumours (most commonly retinal and central nervous system haemangioblastomas, clear cell re...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2011
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3110036/ https://ncbi.nlm.nih.gov/pubmed/21386872 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2010.175 |
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