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2. Turkdogan, Dilsad, Turkyilmaz, Ayberk, Gormez, Zeliha, Sager, Gunes, Ekinci, Gazanfer. 2019. A novel truncating mutation of DOCK7 gene with an early-onset non-encephalopathic epilepsy. In Seizure, 66, 12-14. doi:10.1016/j.seizure.2019.01.010. https://pubmed.ncbi.nlm.nih.gov/30771731/
3. Guo, Gao, Gong, Ke, Beckley, Nicole, Zhao, Dawen, Habib, Amyn A. 2022. EGFR ligand shifts the role of EGFR from oncogene to tumour suppressor in EGFR-amplified glioblastoma by suppressing invasion through BIN3 upregulation. In Nature cell biology, 24, 1291-1305. doi:10.1038/s41556-022-00962-4. https://pubmed.ncbi.nlm.nih.gov/35915159/
4. Mayer, Louisa, Jasztal, Maria, Pardo, Mercedes, Ouwehand, Willem H, Guerrero, Jose A. 2017. Nbeal2 interacts with Dock7, Sec16a, and Vac14. In Blood, 131, 1000-1011. doi:10.1182/blood-2017-08-800359. https://pubmed.ncbi.nlm.nih.gov/29187380/
5. Perrault, Isabelle, Hamdan, Fadi F, Rio, Marlène, Rozet, Jean-Michel, Michaud, Jacques L. 2014. Mutations in DOCK7 in individuals with epileptic encephalopathy and cortical blindness. In American journal of human genetics, 94, 891-7. doi:10.1016/j.ajhg.2014.04.012. https://pubmed.ncbi.nlm.nih.gov/24814191/
6. Yamauchi, Junji, Miyamoto, Yuki, Hamasaki, Hajime, Torii, Tomohiro, Tanoue, Akito. . The atypical Guanine-nucleotide exchange factor, dock7, negatively regulates schwann cell differentiation and myelination. In The Journal of neuroscience : the official journal of the Society for Neuroscience, 31, 12579-92. doi:10.1523/JNEUROSCI.2738-11.2011. https://pubmed.ncbi.nlm.nih.gov/21880919/
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