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Folliculin variants linked to Birt-Hogg-Dubé syndrome are targeted for proteasomal degradation
Germline mutations in the folliculin (FLCN) tumor suppressor gene are linked to Birt-Hogg-Dubé (BHD) syndrome, a dominantly inherited genetic disease characterized by predisposition to fibrofolliculomas, lung cysts, and renal cancer. Most BHD-linked FLCN variants include large deletions and splice s...
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| Publicado no: | PLoS Genet |
|---|---|
| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7660926/ https://ncbi.nlm.nih.gov/pubmed/33137092 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1009187 |
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