A de novo missense mutation in MPP2 confers an increased risk of Vogt-Koyanagi-Harada disease as shown by trio-based whole-exome sequencing.
Liu X, Meng J, Liao X, Liu Y, Zhou Q, Xu Z, Yin S, Cao Q, Su G, He S, Li W, Wang X, Wang G, Li D, Yang P, Hou S.
Liu X, et al. Among authors: wang x, wang g.
Cell Mol Immunol. 2023 Nov;20(11):1379-1392. doi: 10.1038/s41423-023-01088-9. Epub 2023 Oct 12.
Cell Mol Immunol. 2023.
PMID: 37828081
Free PMC article.