TY  - RPRT
TI  - A homozygous human WNT11 loss-of-function variant associated with laterality, heart and renal defects
AU  - Berns, H. E.
AU  - Haas, M.
AU  - Bakey, Z.
AU  - Brislinger-Engelhardt, M. M.
AU  - Schmidts, M.
AU  - Walentek, P.
PY  - 2024
DO  - 10.1101/2024.11.14.623711
UR  - https://www.biorxiv.org/content/10.1101/2024.11.14.623711v1
ID  - 10.1101/2024.11.14.623711
ER  -