1. Fan, Tian-Sin, Wu, Ruey-Meei, Lin, Han-I, Cheng, Chieh, Lin, Chin-Hsien. 2018. PDE8B mutation is not associated with Parkinson's disease in a Taiwanese population. In Neurobiology of aging, 71, 265.e15-265.e16. doi:10.1016/j.neurobiolaging.2018.05.024. https://pubmed.ncbi.nlm.nih.gov/29909144/
2. Mao, Jun, Lu, Mingzhi, Lu, Siduo, Zhou, Jingwen, Du, Wei. 2023. Retinoblastoma gene expression profiling based on bioinformatics analysis. In BMC medical genomics, 16, 101. doi:10.1186/s12920-023-01537-4. https://pubmed.ncbi.nlm.nih.gov/37179305/
3. Tsai, L-C L, Chan, G C-K, Nangle, S N, Beavo, J A, Zweifel, L S. 2012. Inactivation of Pde8b enhances memory, motor performance, and protects against age-induced motor coordination decay. In Genes, brain, and behavior, 11, 837-47. doi:10.1111/j.1601-183X.2012.00836.x. https://pubmed.ncbi.nlm.nih.gov/22925203/
4. Azuma, Reo, Ishikawa, Kinya, Hirata, Kosei, Yokota, Takanori, Orimo, Satoshi. 2015. A novel mutation of PDE8B Gene in a Japanese family with autosomal-dominant striatal degeneration. In Movement disorders : official journal of the Movement Disorder Society, 30, 1964-7. doi:10.1002/mds.26345. https://pubmed.ncbi.nlm.nih.gov/26769607/
5. Agretti, P, De Marco, G, Di Cosmo, C, Vitti, P, Tonacchera, M. 2014. Frequency and effect on serum TSH of phosphodiesterase 8B (PDE8B) gene polymorphisms in patients with sporadic nonautoimmune subclinical hypothyroidism. In Journal of endocrinological investigation, 37, 189-94. doi:10.1007/s40618-013-0036-7. https://pubmed.ncbi.nlm.nih.gov/24497218/
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