1. Gong, Shaoqing, Su, Brenda Bin, Tovar, Hugo, Wang, Ke-Sheng, Xu, Chun. . Polymorphisms Within RYR3 Gene Are Associated With Risk and Age at Onset of Hypertension, Diabetes, and Alzheimer's Disease. In American journal of hypertension, 31, 818-826. doi:10.1093/ajh/hpy046. https://pubmed.ncbi.nlm.nih.gov/29590321/
2. Shrestha, Sadeep, Yan, Qi, Joseph, Gregory, Martinson, Jeremy J, Kingsley, Lawrence A. . Replication of RYR3 gene polymorphism association with cIMT among HIV-infected whites. In AIDS (London, England), 26, 1571-3. doi:10.1097/QAD.0b013e328355359f. https://pubmed.ncbi.nlm.nih.gov/22627881/
3. Garibaldi, Matteo, Rendu, John, Brocard, Julie, Antonini, Giovanni, Romero, Norma Beatriz. 2019. 'Dusty core disease' (DuCD): expanding morphological spectrum of RYR1 recessive myopathies. In Acta neuropathologica communications, 7, 3. doi:10.1186/s40478-018-0655-5. https://pubmed.ncbi.nlm.nih.gov/30611313/
4. O' Donnell, Anne Marie, Nakamura, Hiroki, Puri, Prem. 2019. Altered ryanodine receptor gene expression in Hirschsprung's disease. In Pediatric surgery international, 35, 923-927. doi:10.1007/s00383-019-04504-2. https://pubmed.ncbi.nlm.nih.gov/31263958/
5. Zhao, Chenxi, Ikeda, Shinobu, Arai, Tomio, Muramatsu, Masaaki, Sawabe, Motoji. 2014. Association of the RYR3 gene polymorphisms with atherosclerosis in elderly Japanese population. In BMC cardiovascular disorders, 14, 6. doi:10.1186/1471-2261-14-6. https://pubmed.ncbi.nlm.nih.gov/24423397/
6. Nilipour, Y, Nafissi, S, Tjust, A E, Laing, N G, Tajsharghi, H. 2018. Ryanodine receptor type 3 (RYR3) as a novel gene associated with a myopathy with nemaline bodies. In European journal of neurology, 25, 841-847. doi:10.1111/ene.13607. https://pubmed.ncbi.nlm.nih.gov/29498452/