1. Lin, Yuchen, Xu, Christine L, Velez, Gabriel, Sparrow, Janet R, Tsang, Stephen H. 2019. Novel REEP6 gene mutation associated with autosomal recessive retinitis pigmentosa. In Documenta ophthalmologica. Advances in ophthalmology, 140, 67-75. doi:10.1007/s10633-019-09719-1. https://pubmed.ncbi.nlm.nih.gov/31538292/
2. Son, Yeonho, Choi, Cheoljun, Saha, Abhirup, Granneman, James G, Lee, Yun-Hee. 2022. REEP6 knockout leads to defective β-adrenergic signaling in adipocytes and promotes obesity-related metabolic dysfunction. In Metabolism: clinical and experimental, 130, 155159. doi:10.1016/j.metabol.2022.155159. https://pubmed.ncbi.nlm.nih.gov/35150731/
3. Tseng, Chung-Chih, Hung, Chung-Ching, Shu, Chih-Wen, Ger, Luo-Ping, Liu, Pei-Feng. 2023. The Clinical and Biological Effects of Receptor Expression-Enhancing Protein 6 in Tongue Squamous Cell Carcinoma. In Biomedicines, 11, . doi:10.3390/biomedicines11051270. https://pubmed.ncbi.nlm.nih.gov/37238941/
4. Devlin, Darius J, Agrawal Zaneveld, Smriti, Nozawa, Kaori, Matzuk, Martin M, Chen, Rui. . Knockout of mouse receptor accessory protein 6 leads to sperm function and morphology defects†. In Biology of reproduction, 102, 1234-1247. doi:10.1093/biolre/ioaa024. https://pubmed.ncbi.nlm.nih.gov/32101290/
5. Agrawal, Smriti A, Burgoyne, Thomas, Eblimit, Aiden, Chen, Rui, Cheetham, Michael E. . REEP6 deficiency leads to retinal degeneration through disruption of ER homeostasis and protein trafficking. In Human molecular genetics, 26, 2667-2677. doi:10.1093/hmg/ddx149. https://pubmed.ncbi.nlm.nih.gov/28475715/
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