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FLCN: the causative gene for Birt-Hogg-Dubé syndrome
Germline mutations in the novel tumor suppressor gene FLCN are responsible for the autosomal dominant inherited disorder Birt-Hogg-Dubé (BHD) syndrome that predisposes to fibrofolliculomas, lung cysts and spontaneous pneumothorax, and an increased risk for developing kidney tumors. Although the enco...
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| Publicado no: | Gene |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5682220/ https://ncbi.nlm.nih.gov/pubmed/28970150 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.gene.2017.09.044 |
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