Document is current

Any future updates will be listed below

A de novo missense mutation in MPP2 confers an increased risk of Vogt–Koyanagi–Harada disease as shown by trio-based whole-exome sequencing

Crossref DOI link: https://doi.org/10.1038/s41423-023-01088-9

Published Online: 2023-10-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

About CrossMark