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Driver mutations in USP8 wild-type Cushing’s disease
BACKGROUND: Medical treatment in Cushing’s disease (CD) is limited due to poor understanding of its pathogenesis. Pathogenic variants of ubiquitin specific peptidase 8 (USP8) have been confirmed as causative in around half of corticotroph tumors. We aimed to further characterize the molecular landsc...
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| Yayımlandı: | Neuro Oncol |
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| Asıl Yazarlar: | , , , , , , , , , , , , , , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Oxford University Press
2019
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6784271/ https://ncbi.nlm.nih.gov/pubmed/31222332 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/neuonc/noz109 |
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