1. McKnight, Dianalee, Bean, Lora, Karbassi, Izabela, Zoghbi, Huda, Das, Soma. 2021. Recommendations by the ClinGen Rett/Angelman-like expert panel for gene-specific variant interpretation methods. In Human mutation, 43, 1097-1113. doi:10.1002/humu.24302. https://pubmed.ncbi.nlm.nih.gov/34837432/
2. Bernardo, Pia, Cuccurullo, Claudia, Rubino, Marica, Bilo, Leonilda, Coppola, Antonietta. 2024. X-Linked Epilepsies: A Narrative Review. In International journal of molecular sciences, 25, . doi:10.3390/ijms25074110. https://pubmed.ncbi.nlm.nih.gov/38612920/
3. Figueroa, Karla P, Anderson, Collin J, Paul, Sharan, Scoles, Daniel R, Pulst, Stefan M. . Slc9a6 mutation causes Purkinje cell loss and ataxia in the shaker rat. In Human molecular genetics, 32, 1647-1659. doi:10.1093/hmg/ddad004. https://pubmed.ncbi.nlm.nih.gov/36621975/
4. Wang, Yue, Tian, Xinyao, Wang, Zhecheng, Zheng, Shusen, Yao, Jihong. . A novel peptide encoded by circ-SLC9A6 promotes lipid dyshomeostasis through the regulation of H4K16ac-mediated CD36 transcription in NAFLD. In Clinical and translational medicine, 14, e1801. doi:10.1002/ctm2.1801. https://pubmed.ncbi.nlm.nih.gov/39107881/
5. Mir, Ali, Almudhry, Montaha, Alghamdi, Fouad, Bashir, Shahid, Housawi, Yousef. 2021. SLC gene mutations and pediatric neurological disorders: diverse clinical phenotypes in a Saudi Arabian population. In Human genetics, 141, 81-99. doi:10.1007/s00439-021-02404-x. https://pubmed.ncbi.nlm.nih.gov/34797406/