TY  - RPRT
TI  - Structural analysis and genetic code expansion reveal the functional impact of NR2F1 mutations associated with BBSOA-Syndrome
AU  - Marino, V.
AU  - Phromkrasae, W.
AU  - Bertacchi, M.
AU  - Cassini, P.
AU  - Chakrabandhu, K.
AU  - Dell'Orco, D.
AU  - Studer, M.
PY  - 2023
DO  - 10.1101/2023.07.24.550340
UR  - https://www.biorxiv.org/content/10.1101/2023.07.24.550340v1
ID  - 10.1101/2023.07.24.550340
ER  -