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4. Mroczek, Magdalena, Kabzińska, Dagmara, Chrzanowska, Krystyna H, Pronicki, Maciej, Kochański, Andrzej. 2016. A novel TPM2 gene splice-site mutation causes severe congenital myopathy with arthrogryposis and dysmorphic features. In Journal of applied genetics, 58, 199-203. doi:10.1007/s13353-016-0368-z. https://pubmed.ncbi.nlm.nih.gov/27726070/
5. Hsu, Wei L, Ma, Yun L, Liu, Yen C, Lee, Eminy H Y. 2017. Smad4 SUMOylation is essential for memory formation through upregulation of the skeletal myopathy gene TPM2. In BMC biology, 15, 112. doi:10.1186/s12915-017-0452-9. https://pubmed.ncbi.nlm.nih.gov/29183317/
6. Silva, A Madhushika M, Kennedy, Luke S, Hasan, Stephanie C, Cohen, Alejandro M, Heeley, David H. 2020. Demonstration of beta-tropomyosin (Tpm2) and duplication of the alpha-slow tropomyosin gene (TPM3) in Atlantic salmon Salmo salar. In Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology, 245, 110439. doi:10.1016/j.cbpb.2020.110439. https://pubmed.ncbi.nlm.nih.gov/32283206/
7. Zhou, Xingchen, Li, Zhishuang, Chen, Huan, Zhou, Chengjun, Li, Hui. 2024. Relevance Analysis of TPM2 and Clinicopathological Characteristics in Breast Cancer. In International journal of general medicine, 17, 59-74. doi:10.2147/IJGM.S442004. https://pubmed.ncbi.nlm.nih.gov/38221941/