1. Nieto-Benito, Lula Maria, Suárez-Fernández, Ricardo, Campos-Domínguez, Minia. 2023. A novel pathogenic variation of DOCK6 gene: the genotype-phenotype correlation in Adams-Oliver syndrome. In Molecular biology reports, 50, 5519-5521. doi:10.1007/s11033-023-08430-4. https://pubmed.ncbi.nlm.nih.gov/37133614/
2. Dessay, Mariam, Couture, Emile, Maaroufi, Halim, Brown, Jacques P, Michou, Laëtitia. 2022. Attenuated clinical and osteoclastic phenotypes of Paget's disease of bone linked to the p.Pro392Leu/SQSTM1 mutation by a rare variant in the DOCK6 gene. In BMC medical genomics, 15, 41. doi:10.1186/s12920-022-01198-9. https://pubmed.ncbi.nlm.nih.gov/35241069/
3. Alzahem, Tariq, Alsalamah, Abrar K, Mura, Marco, Alsulaiman, Sulaiman M. 2020. A novel variant in DOCK6 gene associated with Adams-Oliver syndrome type 2. In Ophthalmic genetics, 41, 377-380. doi:10.1080/13816810.2020.1776339. https://pubmed.ncbi.nlm.nih.gov/32498638/
4. Hong, Kai, Cen, Kenan, Chen, Qiaoqiao, Mai, Yifeng, Guo, Yangyang. 2023. Identification and validation of a novel senescence-related biomarker for thyroid cancer to predict the prognosis and immunotherapy. In Frontiers in immunology, 14, 1128390. doi:10.3389/fimmu.2023.1128390. https://pubmed.ncbi.nlm.nih.gov/36761753/
5. Cerikan, Berati, Schiebel, Elmar. 2017. Mechanism of cell-intrinsic adaptation to Adams-Oliver Syndrome gene DOCK6 disruption highlights ubiquitin-like modifier ISG15 as a regulator of RHO GTPases. In Small GTPases, 10, 210-217. doi:10.1080/21541248.2017.1297882. https://pubmed.ncbi.nlm.nih.gov/28287327/
6. Wang, Zhaokun, Wang, Xin, Tang, Xia. 2019. Novel compound heterozygous mutations of the DOCK6 gene in a familial case of Adams-Oliver syndrome 2. In Gene, 700, 65-69. doi:10.1016/j.gene.2019.03.023. https://pubmed.ncbi.nlm.nih.gov/30898718/
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