1. Jeffries, Lauren, Mis, Emily K, McWalter, Kirsty, Lucas, Carrie L, Lakhani, Saquib A. 2023. Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections. In Genetics in medicine : official journal of the American College of Medical Genetics, 26, 101023. doi:10.1016/j.gim.2023.101023. https://pubmed.ncbi.nlm.nih.gov/37947183/
2. Asim, Ambreen, Agarwal, Sarita, Panigrahi, Inusha, Muthuswamy, Srinivasan, Kapoor, Aditya. 2017. CRELD1 gene variants and atrioventricular septal defects in Down syndrome. In Gene, 641, 180-185. doi:10.1016/j.gene.2017.10.044. https://pubmed.ncbi.nlm.nih.gov/29054759/
3. Guo, Ying, Shen, Jie, Yuan, Lang, Wang, Jian, Sun, Kun. 2010. Novel CRELD1 gene mutations in patients with atrioventricular septal defect. In World journal of pediatrics : WJP, 6, 348-52. doi:10.1007/s12519-010-0235-7. https://pubmed.ncbi.nlm.nih.gov/21080147/
4. Beckert, Vera, Rassmann, Sebastian, Kayvanjoo, Amir Hossein, Mass, Elvira, Wachten, Dagmar. 2021. Creld1 regulates myocardial development and function. In Journal of molecular and cellular cardiology, 156, 45-56. doi:10.1016/j.yjmcc.2021.03.008. https://pubmed.ncbi.nlm.nih.gov/33773996/
5. Bonaguro, Lorenzo, Köhne, Maren, Schmidleithner, Lisa, Schultze, Joachim L, Aschenbrenner, Anna C. 2020. CRELD1 modulates homeostasis of the immune system in mice and humans. In Nature immunology, 21, 1517-1527. doi:10.1038/s41590-020-00811-2. https://pubmed.ncbi.nlm.nih.gov/33169013/