1. Mancioppi, Valentina, Daffara, Tommaso, Romanisio, Martina, Giordano, Mara, Prodam, Flavia. 2023. A new mutation in the CAVIN1/PTRF gene in two siblings with congenital generalized lipodystrophy type 4: case reports and review of the literature. In Frontiers in endocrinology, 14, 1212729. doi:10.3389/fendo.2023.1212729. https://pubmed.ncbi.nlm.nih.gov/37501786/
2. Megarbane, Andre, Bizzari, Sami, Deepthi, Asha, Delague, Valérie, Urtizberea, J Andoni. . A 20-year Clinical and Genetic Neuromuscular Cohort Analysis in Lebanon: An International Effort. In Journal of neuromuscular diseases, 9, 193-210. doi:10.3233/JND-210652. https://pubmed.ncbi.nlm.nih.gov/34602496/
3. Al Sayed, Zeina R, Pereira, Céline, Le Borgne, Rémi, Trégouët, David-Alexandre, Hulot, Jean-Sébastien. 2024. CAVIN1-Mediated hERG Dynamics: A Novel Mechanism Underlying the Interindividual Variability in Drug-Induced Long QT. In Circulation, 150, 563-576. doi:10.1161/CIRCULATIONAHA.123.063917. https://pubmed.ncbi.nlm.nih.gov/38682330/
4. Hao, Xingyuan, Li, Jinghua, Liu, Bin, Yuan, Yufeng, Ma, Weijie. 2023. Cavin1 activates the Wnt/β-catenin pathway to influence the proliferation and migration of hepatocellular carcinoma. In Annals of hepatology, 29, 101160. doi:10.1016/j.aohep.2023.101160. https://pubmed.ncbi.nlm.nih.gov/37774837/
5. Akinci, Gulcin, Alyaarubi, Saif, Patni, Nivedita, Akinci, Baris, Garg, Abhimanyu. 2024. Metabolic and other morbid complications in congenital generalized lipodystrophy type 4. In American journal of medical genetics. Part A, 194, e63533. doi:10.1002/ajmg.a.63533. https://pubmed.ncbi.nlm.nih.gov/38234231/
智鼠故事 
