1. Bizzari, Sami, Hamzeh, Abdul Rezzak, Mohamed, Madiha, Al-Ali, Mahmoud Taleb, Bastaki, Fatma. 2019. Expanded PCH1D phenotype linked to EXOSC9 mutation. In European journal of medical genetics, 63, 103622. doi:10.1016/j.ejmg.2019.01.012. https://pubmed.ncbi.nlm.nih.gov/30690203/
2. Fasken, Milo B, Morton, Derrick J, Kuiper, Emily G, Leung, Sara W, Corbett, Anita H. . The RNA Exosome and Human Disease. In Methods in molecular biology (Clifton, N.J.), 2062, 3-33. doi:10.1007/978-1-4939-9822-7_1. https://pubmed.ncbi.nlm.nih.gov/31768969/
3. Yoshino, Seiko, Matsui, Yusuke, Fukui, Yuya, Inoue, Jun-Ichiro, Sakamoto, Takeharu. 2020. EXOSC9 depletion attenuates P-body formation, stress resistance, and tumorigenicity of cancer cells. In Scientific reports, 10, 9275. doi:10.1038/s41598-020-66455-2. https://pubmed.ncbi.nlm.nih.gov/32518284/
4. Sakamoto, Masamune, Iwama, Kazuhiro, Sekiguchi, Futoshi, Miyake, Noriko, Matsumoto, Naomichi. 2020. Novel EXOSC9 variants cause pontocerebellar hypoplasia type 1D with spinal motor neuronopathy and cerebellar atrophy. In Journal of human genetics, 66, 401-407. doi:10.1038/s10038-020-00853-2. https://pubmed.ncbi.nlm.nih.gov/33040083/
5. Noiret, Maud, Mottier, Stéphanie, Angrand, Gaelle, Hardy, Serge, Audic, Yann. 2015. Ptbp1 and Exosc9 knockdowns trigger skin stability defects through different pathways. In Developmental biology, 409, 489-501. doi:10.1016/j.ydbio.2015.11.002. https://pubmed.ncbi.nlm.nih.gov/26546114/
6. Cyske, Zuzanna, Gaffke, Lidia, Pierzynowska, Karolina, Węgrzyn, Grzegorz. 2022. Complex Changes in the Efficiency of the Expression of Many Genes in Monogenic Diseases, Mucopolysaccharidoses, May Arise from Significant Disturbances in the Levels of Factors Involved in the Gene Expression Regulation Processes. In Genes, 13, . doi:10.3390/genes13040593. https://pubmed.ncbi.nlm.nih.gov/35456399/
7. Burns, David T, Donkervoort, Sandra, Müller, Juliane S, Horvath, Rita, Bönnemann, Carsten G. . Variants in EXOSC9 Disrupt the RNA Exosome and Result in Cerebellar Atrophy with Spinal Motor Neuronopathy. In American journal of human genetics, 102, 858-873. doi:10.1016/j.ajhg.2018.03.011. https://pubmed.ncbi.nlm.nih.gov/29727687/
8. Dabaj, Ivana, Hassani, Adnan, Burglen, Lydie, Tebani, Abdellah, Bekri, Soumeya. 2022. Pontocerebellar Hypoplasia Type 1D: A Case Report and Comprehensive Literature Review. In Journal of clinical medicine, 11, . doi:10.3390/jcm11154335. https://pubmed.ncbi.nlm.nih.gov/35893425/
智鼠故事 
