1. Chinta, Vijayendra R, Krishnan, Pramod. 2022. A Novel Mutation of CAPN1 Gene Causing Hereditary Spastic Paraplegia-76. In Annals of Indian Academy of Neurology, 25, 555-558. doi:10.4103/aian.aian_977_21. https://pubmed.ncbi.nlm.nih.gov/35936610/
2. Shu, J T, Zhang, M, Shan, Y J, Chen, K W, Li, H F. 2015. Analysis of the genetic effects of CAPN1 gene polymorphisms on chicken meat tenderness. In Genetics and molecular research : GMR, 14, 1393-403. doi:10.4238/2015.February.13.18. https://pubmed.ncbi.nlm.nih.gov/25730078/
3. Peng, Fang, Sun, Yi-Min, Quan, Chao, Wang, Jian, Wu, Jian-Jun. 2019. Two novel homozygous mutations of CAPN1 in Chinese patients with hereditary spastic paraplegia and literatures review. In Orphanet journal of rare diseases, 14, 83. doi:10.1186/s13023-019-1053-1. https://pubmed.ncbi.nlm.nih.gov/31023339/
4. Liu, Yueyang, Che, Xiaohang, Zhang, Haotian, Yang, Jingyu, Zhou, Ming-Sheng. 2021. CAPN1 (Calpain1)-Mediated Impairment of Autophagic Flux Contributes to Cerebral Ischemia-Induced Neuronal Damage. In Stroke, 52, 1809-1821. doi:10.1161/STROKEAHA.120.032749. https://pubmed.ncbi.nlm.nih.gov/33874744/
5. Su, Wenyue, Zhou, Qian, Wang, Yubin, Bi, Xiaoning, Baudry, Michel. 2020. Deletion of the Capn1 Gene Results in Alterations in Signaling Pathways Related to Alzheimer's Disease, Protein Quality Control and Synaptic Plasticity in Mouse Brain. In Frontiers in genetics, 11, 334. doi:10.3389/fgene.2020.00334. https://pubmed.ncbi.nlm.nih.gov/32328086/
6. Rasouli, Z, Zerehdaran, S, Azari, M A, Shargh, M S. . Genetic polymorphism of the CAPN1 gene is associated with meat quality traits in Japanese quail. In British poultry science, 54, 171-5. doi:10.1080/00071668.2013.770128. https://pubmed.ncbi.nlm.nih.gov/23647179/
7. Zhou, Yu-Guang, Xiong, Yong, Yang, Chao-Wu, Hu, Yao-Dong, Liu, Yi-Ping. 2017. Experimental Verification of CAPN1 and CAST Gene Polymorphisms in Different Generations of Da-Heng Broilers. In BioMed research international, 2017, 7968450. doi:10.1155/2017/7968450. https://pubmed.ncbi.nlm.nih.gov/28713829/
8. Lai, Lu-Lu, Chen, Yi-Jun, Li, Yun-Lu, Chen, Wan-Jin, Lin, Xiang. 2020. Novel CAPN1 mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia. In Annals of clinical and translational neurology, 7, 1862-1869. doi:10.1002/acn3.51169. https://pubmed.ncbi.nlm.nih.gov/32860341/