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. 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/
4. 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/
5. Mass, Elvira, Wachten, Dagmar, Aschenbrenner, Anna C, Voelzmann, André, Hoch, Michael. . Murine Creld1 controls cardiac development through activation of calcineurin/NFATc1 signaling. In Developmental cell, 28, 711-26. doi:10.1016/j.devcel.2014.02.012. https://pubmed.ncbi.nlm.nih.gov/24697899/
6. Robinson, Susan W, Morris, Cynthia D, Goldmuntz, Elizabeth, Steiner, Robert D, Maslen, Cheryl L. 2003. Missense mutations in CRELD1 are associated with cardiac atrioventricular septal defects. In American journal of human genetics, 72, 1047-52. doi:. https://pubmed.ncbi.nlm.nih.gov/12632326/
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