Genetica degli adenomi ACTH secernenti: mutazioni somatiche
Author:
Publisher
Springer Science and Business Media LLC
Subject
Microbiology
Link
https://link.springer.com/content/pdf/10.1007/s40619-023-01400-9.pdf
Reference8 articles.
1. Wanichi IQ, de Paula Mariani BM, Frassetto FP et al. (2019) Cushing’s disease due to somatic USP8 mutations: a systematic review and meta-analysis. Pituitary 22(4):435–442
2. Albani A, Pérez-Rivas LG, Dimopoulou C et al. (2018) The USP8 mutational status may predict long-term remission in patients with Cushing’s disease. Clin Endocrinol. https://doi.org/10.1111/cen.13802
3. Chen J, Jian X, Deng S et al. (2018) Identification of recurrent USP48 and BRAF mutations in Cushing’s disease. Nat Commun 9(1):3171
4. Sbiera S, Perez-Rivas LG, Taranets L et al. (2019) Driver mutations in USP8 wild-type Cushing’s disease. Neuro-Oncol 21(10):1273–1283
5. Abraham AP, Pai R, Beno DL et al. (2022) USP8, USP48, and BRAF mutations differ in their genotype-phenotype correlation in Asian Indian patients with Cushing’s disease. Endocrine 75(2):549–559
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