1. Bilal, Muhammad, Khan, Hammal, Khan, Muhammad Javed, Ahmad, Wasim, Leal, Suzanne M. 2023. Variants in EFCAB7 underlie nonsyndromic postaxial polydactyly. In European journal of human genetics : EJHG, 31, 1270-1274. doi:10.1038/s41431-023-01450-5. https://pubmed.ncbi.nlm.nih.gov/37684519/
2. Fish, Eric W, Boschen, Karen E, Parnell, Scott E. 2024. Efcab7 deletion sensitizes mice to the teratogenic effects of gastrulation-stage alcohol exposure. In Reproductive toxicology (Elmsford, N.Y.), 130, 108729. doi:10.1016/j.reprotox.2024.108729. https://pubmed.ncbi.nlm.nih.gov/39366525/
3. Cui, Dan, Wang, Hongye, Wang, Zhi, Chi, Jiachang, Zhai, Bo. 2024. Upregulation of EFCAB7 after radiofrequency ablation promoting hepatocellular carcinoma metastasis and survival by regulating PARK7. In Aging, 16, 12252-12262. doi:10.18632/aging.206073. https://pubmed.ncbi.nlm.nih.gov/39276379/
4. Yang, Xin, Wang, Qiuye, Li, Tianyuan, Yue, Shen, Hu, Zhibin. 2025. A splicing variant in EFCAB7 hinders ciliary transport and disrupts cardiac development. In The Journal of biological chemistry, 301, 108249. doi:10.1016/j.jbc.2025.108249. https://pubmed.ncbi.nlm.nih.gov/39894222/
5. Pusapati, Ganesh V, Hughes, Casey E, Dorn, Karolin V, Aravind, L, Rohatgi, Rajat. 2014. EFCAB7 and IQCE regulate hedgehog signaling by tethering the EVC-EVC2 complex to the base of primary cilia. In Developmental cell, 28, 483-96. doi:10.1016/j.devcel.2014.01.021. https://pubmed.ncbi.nlm.nih.gov/24582806/
6. Nguyen, Tran Quynh Nhu, Saitoh, Makiko, Trinh, Huu Tung, Ogawa, Seishi, Mizuguchi, Masashi. . Truncation and microdeletion of EVC/EVC2 with missense mutation of EFCAB7 in Ellis-van Creveld syndrome. In Congenital anomalies, 56, 209-16. doi:10.1111/cga.12155. https://pubmed.ncbi.nlm.nih.gov/26748586/
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