Structural analysis and genetic code expansion reveal the functional impact of NR2F1 mutations associated with BBSOA-Syndrome https://www.biorxiv.org/content/10.1101/2023.07.24.550340v1?med=mas
Structural analysis and genetic code expansion reveal the functional impact of NR2F1 mutations associated with BBSOA-Syndrome https://www.biorxiv.org/content/10.1101/2023.07.24.550340v1?med=mas