1. Zhao, Tianyun, Zhao, Junji, Ma, Chi, Wei, Bo, Liu, Jibin. . Common variants in LTBP3 gene contributed to the risk of hip osteoarthritis in Han Chinese population. In Bioscience reports, 40, . doi:10.1042/BSR20192999. https://pubmed.ncbi.nlm.nih.gov/32452514/
2. Hadid, Yarin, Daher, Ziad, Mahroum, Mohammad, Levitaz, Jasmin, Shalata, Adel. . [IDENTIFICATION OF A NOVEL LTBP3 GENE PATHOGENIC VARIANT IN DRUZE ARAB PATIENTS PRESENTED WITH SYNDROMIC SHORT STATURE WITH BRACHYOLMIA AND AMELOGENESIS IMPERFECTA]. In Harefuah, 162, 352-358. doi:. https://pubmed.ncbi.nlm.nih.gov/37394436/
3. Zhu, Guoyan, Luo, Mingyao, Chen, Qianlong, Yang, Hang, Zhou, Zhou. 2021. Novel LTBP3 mutations associated with thoracic aortic aneurysms and dissections. In Orphanet journal of rare diseases, 16, 513. doi:10.1186/s13023-021-02143-2. https://pubmed.ncbi.nlm.nih.gov/34906192/
4. Li, Bingzong, Chen, Ping, Qu, Jing, Sun, Yu, Zhuang, Wenzhuo. 2014. Activation of LTBP3 gene by a long noncoding RNA (lncRNA) MALAT1 transcript in mesenchymal stem cells from multiple myeloma. In The Journal of biological chemistry, 289, 29365-75. doi:10.1074/jbc.M114.572693. https://pubmed.ncbi.nlm.nih.gov/25187517/
5. Rudd Garces, Gabriela, Knebel, Anna, Hülskötter, Kirsten, Leeb, Tosso, Volk, Holger A. 2021. LTBP3 Frameshift Variant in British Shorthair Cats with Complex Skeletal Dysplasia. In Genes, 12, . doi:10.3390/genes12121923. https://pubmed.ncbi.nlm.nih.gov/34946872/
6. Noor, Abdul, Windpassinger, Christian, Vitcu, Irina, Alman, Benjamin, Vincent, John B. 2009. Oligodontia is caused by mutation in LTBP3, the gene encoding latent TGF-beta binding protein 3. In American journal of human genetics, 84, 519-23. doi:10.1016/j.ajhg.2009.03.007. https://pubmed.ncbi.nlm.nih.gov/19344874/
7. Deryugina, Elena I, Zajac, Ewa, Zilberberg, Lior, Rifkin, Daniel, Quigley, James P. 2018. LTBP3 promotes early metastatic events during cancer cell dissemination. In Oncogene, 37, 1815-1829. doi:10.1038/s41388-017-0075-1. https://pubmed.ncbi.nlm.nih.gov/29348457/
8. Huckert, Mathilde, Stoetzel, Corinne, Morkmued, Supawich, Dollfus, Hélène, Bloch-Zupan, Agnès. 2015. Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta. In Human molecular genetics, 24, 3038-49. doi:10.1093/hmg/ddv053. https://pubmed.ncbi.nlm.nih.gov/25669657/
9. Guo, Dong-Chuan, Regalado, Ellen S, Pinard, Amelie, Rifkin, Daniel B, Milewicz, Dianna M. . LTBP3 Pathogenic Variants Predispose Individuals to Thoracic Aortic Aneurysms and Dissections. In American journal of human genetics, 102, 706-712. doi:10.1016/j.ajhg.2018.03.002. https://pubmed.ncbi.nlm.nih.gov/29625025/
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